396-31-6|3-Fluoroquinoline| Ambeed

Size	Price	VIP Price	US Stock	Global Stock	In Stock
{[ item.pr_size ]}		Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

{[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

Quality Control of [ 396-31-6 ] Purity: 95% SDS Specification

COA

Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.

NMR

Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.

CNMR

Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.

HPLC

Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.

LC-MS

Search for reports by entering the product batch number.
Batch number can be found on the product's label following the word 'Batch'.

1-2 Day Shipping
High Quality
Technical Support

Product Details of [ 396-31-6 ]

CAS No. :	396-31-6
Formula :	C₉H₆FN
M.W :	147.15
SMILES Code :	FC1=CC2=CC=CC=C2N=C1
MDL No. :	MFCD00234493
InChI Key :	UFIGOYSEDNHKGT-UHFFFAOYSA-N
Pubchem ID :	96405

Safety of [ 396-31-6 ]

GHS Pictogram:
Signal Word:	Warning
Hazard Statements:	H302-H315-H320-H335
Precautionary Statements:	P264-P270-P301+P312-P330

Computational Chemistry of [ 396-31-6 ] Show Less

Physicochemical Properties

Num. heavy atoms	11
Num. arom. heavy atoms	10
Fraction Csp3	0.0
Num. rotatable bonds	0
Num. H-bond acceptors	2.0
Num. H-bond donors	0.0
Molar Refractivity	41.7
TPSA ? Topological Polar Surface Area: Calculated from Ertl P. et al. 2000 J. Med. Chem.	12.89 Å²

Lipophilicity

Log P_o/w (iLOGP)? iLOGP: in-house physics-based method implemented from Daina A et al. 2014 J. Chem. Inf. Model.	1.89
Log P_o/w (XLOGP3)? XLOGP3: Atomistic and knowledge-based method calculated by XLOGP program, version 3.2.2, courtesy of CCBG, Shanghai Institute of Organic Chemistry	2.41
Log P_o/w (WLOGP)? WLOGP: Atomistic method implemented from Wildman SA and Crippen GM. 1999 J. Chem. Inf. Model.	2.79
Log P_o/w (MLOGP)? MLOGP: Topological method implemented from Moriguchi I. et al. 1992 Chem. Pharm. Bull. Moriguchi I. et al. 1994 Chem. Pharm. Bull. Lipinski PA. et al. 2001 Adv. Drug. Deliv. Rev.	2.27
Log P_o/w (SILICOS-IT)? SILICOS-IT: Hybrid fragmental/topological method calculated by FILTER-IT program, version 1.0.2, courtesy of SILICOS-IT, http://www.silicos-it.com	2.91
Consensus Log P_o/w? Consensus Log P_o/w: Average of all five predictions	2.45

Water Solubility

Log S (ESOL):? ESOL: Topological method implemented from Delaney JS. 2004 J. Chem. Inf. Model.	-2.94
Solubility	0.168 mg/ml ; 0.00114 mol/l
Class? Solubility class: Log S scale Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly	Soluble
Log S (Ali)? Ali: Topological method implemented from Ali J. et al. 2012 J. Chem. Inf. Model.	-2.32
Solubility	0.7 mg/ml ; 0.00476 mol/l
Class? Solubility class: Log S scale Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly	Soluble
Log S (SILICOS-IT)? SILICOS-IT: Fragmental method calculated by FILTER-IT program, version 1.0.2, courtesy of SILICOS-IT, http://www.silicos-it.com	-3.96
Solubility	0.0162 mg/ml ; 0.00011 mol/l
Class? Solubility class: Log S scale Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly	Soluble

Pharmacokinetics

GI absorption? Gatrointestinal absorption: according to the white of the BOILED-Egg	High
BBB permeant? BBB permeation: according to the yolk of the BOILED-Egg	Yes
P-gp substrate? P-glycoprotein substrate: SVM model built on 1033 molecules (training set) and tested on 415 molecules (test set) 10-fold CV: ACC=0.72 / AUC=0.77 External: ACC=0.88 / AUC=0.94	No
CYP1A2 inhibitor? Cytochrome P450 1A2 inhibitor: SVM model built on 9145 molecules (training set) and tested on 3000 molecules (test set) 10-fold CV: ACC=0.83 / AUC=0.90 External: ACC=0.84 / AUC=0.91	Yes
CYP2C19 inhibitor? Cytochrome P450 2C19 inhibitor: SVM model built on 9272 molecules (training set) and tested on 3000 molecules (test set) 10-fold CV: ACC=0.80 / AUC=0.86 External: ACC=0.80 / AUC=0.87	No
CYP2C9 inhibitor? Cytochrome P450 2C9 inhibitor: SVM model built on 5940 molecules (training set) and tested on 2075 molecules (test set) 10-fold CV: ACC=0.78 / AUC=0.85 External: ACC=0.71 / AUC=0.81	No
CYP2D6 inhibitor? Cytochrome P450 2D6 inhibitor: SVM model built on 3664 molecules (training set) and tested on 1068 molecules (test set) 10-fold CV: ACC=0.79 / AUC=0.85 External: ACC=0.81 / AUC=0.87	No
CYP3A4 inhibitor? Cytochrome P450 3A4 inhibitor: SVM model built on 7518 molecules (training set) and tested on 2579 molecules (test set) 10-fold CV: ACC=0.77 / AUC=0.85 External: ACC=0.78 / AUC=0.86	No
Log Kp (skin permeation)? Skin permeation: QSPR model implemented from Potts RO and Guy RH. 1992 Pharm. Res.	-5.49 cm/s

Druglikeness

Lipinski? Lipinski (Pfizer) filter: implemented from Lipinski CA. et al. 2001 Adv. Drug Deliv. Rev. MW ≤ 500 MLOGP ≤ 4.15 N or O ≤ 10 NH or OH ≤ 5	0.0
Ghose? Ghose filter: implemented from Ghose AK. et al. 1999 J. Comb. Chem. 160 ≤ MW ≤ 480 -0.4 ≤ WLOGP ≤ 5.6 40 ≤ MR ≤ 130 20 ≤ atoms ≤ 70	None
Veber? Veber (GSK) filter: implemented from Veber DF. et al. 2002 J. Med. Chem. Rotatable bonds ≤ 10 TPSA ≤ 140	0.0
Egan? Egan (Pharmacia) filter: implemented from Egan WJ. et al. 2000 J. Med. Chem. WLOGP ≤ 5.88 TPSA ≤ 131.6	0.0
Muegge? Muegge (Bayer) filter: implemented from Muegge I. et al. 2001 J. Med. Chem. 200 ≤ MW ≤ 600 -2 ≤ XLOGP ≤ 5 TPSA ≤ 150 Num. rings ≤ 7 Num. carbon > 4 Num. heteroatoms > 1 Num. rotatable bonds ≤ 15 H-bond acc. ≤ 10 H-bond don. ≤ 5	2.0
Bioavailability Score? Abbott Bioavailability Score: Probability of F > 10% in rat implemented from Martin YC. 2005 J. Med. Chem.	0.55

Medicinal Chemistry

PAINS? Pan Assay Interference Structures: implemented from Baell JB. & Holloway GA. 2010 J. Med. Chem.	0.0 alert
Brenk? Structural Alert: implemented from Brenk R. et al. 2008 ChemMedChem	0.0 alert: heavy_metal
Leadlikeness? Leadlikeness: implemented from Teague SJ. 1999 Angew. Chem. Int. Ed. 250 ≤ MW ≤ 350 XLOGP ≤ 3.5 Num. rotatable bonds ≤ 7	No; 1 violation:MW<1.0
Synthetic accessibility? Synthetic accessibility score: from 1 (very easy) to 10 (very difficult) based on 1024 fragmental contributions (FP2) modulated by size and complexity penaties, trained on 12'782'590 molecules and tested on 40 external molecules (r² = 0.94)	1.37

Application In Synthesis of [ 396-31-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

Downstream synthetic route of [ 396-31-6 ]

[ 396-31-6 ] Synthesis Path-Downstream 1~35

1
[ 396-31-6 ]
[ 74-88-4 ]
[ 84078-57-9 ]

References: [1]Organic Magnetic Resonance,1982,vol. 20,p. 92 - 101.

2
[ 580-17-6 ]
[ 396-31-6 ]

Yield	Reaction Conditions	Operation in experiment
40%	With tert.-butylnitrite; boron trifluoride; In chlorobenzene; at 50 - 100℃; for 1.5h;	Example 11 Preparation of 3-fluoroquinoline 1 g (6.94 mmol) of 3-aminoquinoline in 10 ml of chlorobenzene is introduced dropwise over 10 minutes onto a heel of 0.66 ml (10.4 mmol, 1.5 mol. eq.) of BF3.2H2O at ambient temperature in a 50 ml three-necked flask equipped with a reflux condenser, a thermocouple and a stirring system. The reaction medium is then heated to 50 C. and then 1.2 ml (9.01 mmol, 1.3 mol. eq.) of t-butyl nitrite (purity 90%) are added at this temperature over 30 minutes. The reaction medium is brought to 100 C. and stirred for 1 hour. The yield of isolated product is 40%.
	With tetrafluoroboric acid; sodium bicarbonate; sodium nitrite; In diethyl ether; ethanol; water; ethyl acetate; toluene; Petroleum ether;	3-Fluoroquinoline 23.5 g of 3-aminoquinoline and 12.1 g of sodium nitrite in 20 cm3 of distilled water were added cautiously to 100 cm3 of tetrafluoroboric acid cooled to about 0 C., with vigorous stirring, and the reaction mixture was thus stirred for 30 minutes. The suspension was filtered, spin-filtered, washed with 3 times 30 cm3 of ice-cold tetrafluoroboric acid, 50 cm3 of ice-cold ethanol and 4 times 30 cm3 of diethyl ether. The solid was dried in a desiccator (2 kPa) in the region of 20 C. and then taken up in 200 cm3 of toluene and heated at a temperature in the region of 90 C. for 1 hour with stirring. After cooling to about 20 C., the phases of the reaction mass were separated by settling and the insoluble oil was washed with 3 times 100 cm3 of toluene and taken up in 110 cm3 of water, which was basified by slow addition of sodium hydrogen carbonate so that the pH was at about 8. The aqueous phase was extracted with 5 times 100 cm3 of diethyl ether and the organic phases were combined, washed with twice 50 cm3 of water, dried over magnesium sulfate and taken up with vegetable charcoal (3S), filtered and concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 45 C. The oil was taken up in 50 cm3 of a 40-60 C. petroleum ether/ethyl acetate mixture (90/10 by volume) and the insoluble material was filtered off, rinsed with twice 25 cm3 of a 40-60 C. petroleum ether/ethyl acetate mixture (90/10 by volume) and dried in a desiccator under reduced pressure (2 kPa) at a temperature in the region of 20 C. The filtrate was concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40 C. The residue obtained was purified by chromatography under atmospheric pressure, on a column of silica gel (particle size 20-45 μ; diameter 5 cm; height 45 cm), eluding with a 40-60 C. petroleum ether/ethyl acetate mixture (90/10 by volume) and collecting 100-cm3 fractions. Fractions 20 to 31 were combined and then concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40 C. 13 g of 3-fluoroquinoline were obtained in the form of a colorless liquid. Mass spectrum: EI m/z=147 M+. base peak m/z=127 [M-HF]+. m/z=120 [M-HCN]+
	With tert.-butylnitrite; boron trifluoride diethyl etherate; In 1,2-dichloro-benzene; at 100℃; for 1h;	Tert-butylnitrite (4.6 ml, 38.7 mmol) was added dropwise over 15 min to a solution of quinolin-3 -amine (4.61 g, 32.0 mmol) and borontrifluoride-etherate (6 ml, 47.3 mmol) in dichlorobenzene (100 ml). The solution was heated to 100C. After stirring for for 1 h, the solution was cooled to ambient temperature and the dichlorobenzene was decanted leaving 3-fluoroquinoline as a black residue. Method [8] retention time 3.28 min by HPLC (M+ 148).

1.6 g	With tetrafluoroboric acid; sodium nitrite; In water; at 0 - 20℃; for 1h;	Quinolin-3 -amine (4 g, 27.7 mmol) was added to HBF4 (26 mL, 48 % aqueous solution) portionwise at room temperature, and the mixture was stirred at room temperature until it became homogeneous. The mixture was then cooled to 0C, and a solution of NaN02 (2.4 g, 34.8 mmol) in H20 (8 mL) was added dropwise, when the reaction mixture became heterogeneous. The mixture was stirred at 0C for 1 hour, then the mixture was filtered, and the filtered cake was washed with cold EtOH, then Et20. The resulting solid was dried under vacuum, then suspended in toluene in a round bottom flask and was refluxed for 1.5 hours. The resulting mixture was cooled to room temperature, and then poured into cold water. The organic layer was dried over Na2S04, and then concentrated in vacuo to obtain the desired product (1.6 g). LC-MS: m/z 148.1 (M+H)+
1.6 g		Quinolin-3-amine (4 g, 27.7 mmol) was added to HBF4 (26 mL, 48% aqueous solution) portionwise at room temperature, and the mixture was stirred at room temperature until it became homogeneous. The mixture was then cooled to 0 C., and a solution of NaNO2 (2.4 g, 34.8 mmol) in H2O (8 mL) was added dropwise, when the reaction mixture became heterogeneous. The mixture was stirred at 0 C. for 1 hour, then the mixture was filtered, and the filtered cake was washed with cold EtOH, then Et2O. The resulting solid was dried under vacuum, then suspended in toluene in a round bottom flask and was refluxed for 1.5 hours. The resulting mixture was cooled to room temperature, and then poured into cold water. The organic layer was dried over Na2SO4, and then concentrated in vacuo to obtain the desired product (1.6 g). LC-MS: m/z 148.1 (M+H)+
1.6 g	With tetrafluoroboric acid; sodium nitrite; In water; at 0 - 20℃; for 1h;	Quinolin-3 -amine (4 g, 27.7 mmol) was added to HBF4 (26 mL, 48 % aqueous solution) portionwise at room temperature, and the mixture was stirred at room temperature until it became homogeneous. The mixture was then cooled to 0C, and a solution of NaN02 (2.4 g, 34.8 mmol) in H20 (8 mL) was added dropwise, when the reaction mixture became heterogeneous. The mixture was stirred at 0C for 1 hour, then the mixture was filtered, and the filtered cake was washed with cold EtOH, then Et20. The resulting solid was dried under vacuum, then suspended in toluene in a round bottom flask and was refluxed for 1.5 hours. The resulting mixture was cooled to room temperature, and then poured into cold water. The organic layer was dried over Na2S04, and then concentrated in vacuo to obtain the desired product (1.6 g). LC-MS: m/z 148.1 (M+H)+

References: [1]Journal of Medicinal Chemistry,2016,vol. 59,p. 264 - 281.
[2]Journal of Medicinal Chemistry,2010,vol. 53,p. 4066 - 4084.
[3]Tetrahedron Letters,2006,vol. 47,p. 5705 - 5708.
[4]Patent: US2007/276168,2007,A1 .Location in patent: Page/Page column 9.
[5]Organic Magnetic Resonance,1982,vol. 20,p. 92 - 101.
[6]Patent: US2002/111492,2002,A1 .
[7]Patent: WO2010/91310,2010,A1 .Location in patent: Page/Page column 146.
[8]Patent: WO2014/139144,2014,A1 .Location in patent: Page/Page column 178.
[9]Patent: US2014/288081,2014,A1 .Location in patent: Paragraph 0733; 0734.
[10]Patent: WO2014/139325,2014,A1 .Location in patent: Page/Page column 191; 192.
[11]Angewandte Chemie - International Edition,2018,vol. 57,p. 9896 - 9900.
Angew. Chem.,2018,vol. 130,p. 10044 - 10048,5.

3
[ 124467-21-6 ]
[ 396-31-6 ]

References: [1]Tetrahedron,1994,vol. 50,p. 1129 - 1134.

4
[ 396-31-6 ]
[ 191861-20-8 ]
3-fluoro-8-nitroquinoline [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
	With sulfuric acid; nitric acid; at 0℃; for 2h;	A solution of 3: 1 concentrated sulfuric acid/concentrated nitric acid (32 ml) was added dropwise to <strong>[396-31-6]3-fluoroquinoline</strong> (13.04 g, 88.6 mmol) in concentrated sulfuric acid (100 ml) at 00C. After stirring for 2 h, the solution was made alkaline with IO N aq. NaOH and extracted with diethyl ether. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated under reduced pressure to yield 3-fluoro-8-nitroquinoline and 3-fluoro- 5-nitroquinoline as a yellow solid. Method [7] retention time 3.50 and 3.92 min by HPLC (M+ 193) and (M+ 193).

References: [1]Mutation Research - Genetic Toxicology and Environmental Mutagenesis,1999,vol. 441,p. 205 - 213.
[2]Journal of Medicinal Chemistry,2010,vol. 53,p. 4066 - 4084.
[3]Patent: WO2010/91310,2010,A1 .Location in patent: Page/Page column 146.

7
quinoline-3-diazonium-tetrafluoroborate [ No CAS ]
[ 396-31-6 ]

References: [1]Journal of the American Chemical Society,1949,vol. 71,p. 1785.

8
[ 396-31-6 ]
LIC-KOR reagent [ No CAS ]
3-fluoro-4-quinolinecarboxylic acid [ No CAS ]

References: [1]Tetrahedron,1994,vol. 50,p. 1129 - 1134.

9
[ 396-31-6 ]
[ 213772-63-5 ]

Yield	Reaction Conditions	Operation in experiment
	With n-butyllithium; iodine; diisopropylamine; In tetrahydrofuran; hexane; ethyl acetate;	3-Fluoro-4-iodoquinoline 17.3 cm3 of diisopropylamine in 650 cm3 of tetrahydrofuran were cooled to a temperature in the region of -75 C. and 76 cm3 of a 1.6M solution of butyl lithium in hexane were added, with stirring and under an inert atmosphere, while maintaining the temperature at about -70 C. After stirring for 20 minutes at a temperature in the region of -75 C., a solution of 11.9 g of <strong>[396-31-6]3-fluoroquinoline</strong> in 200 cm3 of tetrahydrofuran was added. The solution obtained was stirred for a further 4 hours at -75 C., followed by addition of a solution of 32.2 g of double-sublimed iodine in 150 cm3 of tetrahydrofuran. After stirring for 2 hours at a temperature in the region of -40 C., the reaction mixture was hydrolyzed with 200 cm3 of a tetrahydrofuran/water mixture (90/10 by volume) and then with 200 cm3 of saturated sodium chloride solution. In the region of 20 C., the mixture was diluted with 300 cm3 of ethyl acetate and washed with twice 250 cm3 of saturated sodium chloride solution. The organic phase was dried over magnesium sulfate, filtered and concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 50C. The residue obtained was purified by chromatography under atmospheric pressure, on a column of silica gel (particle size 20-45 μ; diameter 10 cm; height 30 cm), eluding with dichloromethane and collecting 100-cm3 fractions. Fractions 45 to 80 were combined and then concentrated to dryness under reduced pressure (2 kPa) at a temperature in the region of 40 C. 15.1 g of 3-fluoro-4-iodoquinoline were obtained in the form of a cream-colored solid melting at 110 C. Mass spectrum: EI m/z=273 M+. base peak m/z 146 [M-I]+

References: [1]Tetrahedron,1999,vol. 55,p. 12149 - 12156.
[2]Journal of Medicinal Chemistry,2016,vol. 59,p. 264 - 281.
[3]Patent: US2002/111492,2002,A1 .

10
[ 396-31-6 ]
[ 191861-20-8 ]

References: [1]Biological and Pharmaceutical Bulletin,1997,vol. 20,p. 646 - 650.

11
[ 396-31-6 ]
[ 1479-96-5 ]

References: [1]Synthesis,2001,p. 2495 - 2499.

12
[ 396-31-6 ]
[ 100-59-4 ]
[ 1666-96-2 ]

References: [1]Journal of Organic Chemistry,2002,vol. 67,p. 8991 - 8994.

13
[ 396-31-6 ]
3,3'-difluoro-[2,2']biquinolinyl [ No CAS ]

References: [1]Tetrahedron Letters,2004,vol. 45,p. 6697 - 6701.

14
[ 834883-99-7 ]
[ 396-31-6 ]

References: [1]Tetrahedron,2005,vol. 61,p. 717 - 725.

15
[ 124467-22-7 ]
[ 396-31-6 ]

References: [1]Tetrahedron,2005,vol. 61,p. 717 - 725.
[2]Tetrahedron,1994,vol. 50,p. 1129 - 1134.

16
[ 396-31-6 ]
3,5-Difluoroquinoline [ No CAS ]

References: [1]Biological and Pharmaceutical Bulletin,1997,vol. 20,p. 646 - 650.

17
[ 396-31-6 ]
[ 155014-05-4 ]

References: [1]Biological and Pharmaceutical Bulletin,1997,vol. 20,p. 646 - 650.

18
[ 396-31-6 ]
9-Fluoro-1,7-phenanthroline [ No CAS ]

References: [1]Biological and Pharmaceutical Bulletin,1997,vol. 20,p. 646 - 650.

19
[ 396-31-6 ]
[ 191861-21-9 ]

References: [1]Biological and Pharmaceutical Bulletin,1997,vol. 20,p. 646 - 650.

20
[ 396-31-6 ]
[ 250739-99-2 ]

References: [1]Tetrahedron,1999,vol. 55,p. 12149 - 12156.

21
[ 396-31-6 ]
[ 250740-01-3 ]

References: [1]Tetrahedron,1999,vol. 55,p. 12149 - 12156.

22
[ 396-31-6 ]
[ 250740-00-2 ]

References: [1]Tetrahedron,1999,vol. 55,p. 12149 - 12156.

23
[ 396-31-6 ]
8-fluoro-N-methyl-5-nitroquinoline methanesulfonate [ No CAS ]

References: [1]Mutation Research - Genetic Toxicology and Environmental Mutagenesis,1999,vol. 441,p. 205 - 213.

24
[ 396-31-6 ]
3-fluoro-N-methyl-5-nitroquinoline methanesulfonate [ No CAS ]

References: [1]Mutation Research - Genetic Toxicology and Environmental Mutagenesis,1999,vol. 441,p. 205 - 213.

25
[ 62-53-3 ]
p-toluenesulfonic acid-<p-amino-phenyl>-ester [ No CAS ]
[ 396-31-6 ]

References: [1]Tetrahedron,1994,vol. 50,p. 1129 - 1134.

26
[ 175609-72-0 ]
[ 396-31-6 ]

References: [1]Tetrahedron,1994,vol. 50,p. 1129 - 1134.

27
[ 396-31-6 ]
[ 846038-33-3 ]
[ 155014-05-4 ]

Yield	Reaction Conditions	Operation in experiment
11%; 37%		A solution of 3: 1 concentrated sulfuric acid/concentrated nitric acid (32 ml) was added dropwise to <strong>[396-31-6]3-fluoroquinoline</strong> (13.04 g, 88.6 mmol) in concentrated sulfuric acid (100 ml) at 00C. After stirring for 2 h, the solution was made alkaline with IO N aq. NaOH and extracted with diethyl ether. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated under reduced pressure to yield 3-fluoro-8-nitroquinoline and 3-fluoro- 5-nitroquinoline as a yellow solid. Method [7] retention time 3.50 and 3.92 min by HPLC (M+ 193) and (M+ 193).3-Fluoro-8-nitroquinoline, 3-fluoro-5-nitroquinoline, and tin(II)chloride- dihydrate (68.23 g, 302 mmol) in ethyl acetate (200 ml) was placed into a preheated oil bath at 600C. After heating for 4 h, the solution was cooled to ambient temperature, diluted with 3 N aq. NaOH, and filtered through a pad of celite. The filtrate was extracted with ethyl acetate, the combined organic extracts were dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was flash chromatographed with 19: 1, 9: 1, 17:3, 4: 1, 3: 1, 7:3, and 3:2 hexane:ethyl acetate as the eluant to afford 2.14 g (11% yield over two steps) 3- fluoroquinolin-8-amine and 7.02 g (37% yield over two steps) of 3-fluoroquinolin-5-amine. Method [6] retention time 1.57 and 4.02 min by HPLC (M+ 163) and (M+ 163).

References: [1]Patent: WO2010/91310,2010,A1 .Location in patent: Page/Page column 146.
[2]Journal of Medicinal Chemistry,2010,vol. 53,p. 4066 - 4084.

28
quinolin-3-yl trifluoromethanesulfonate [ No CAS ]
[ 396-31-6 ]

References: [1]Organic Letters,2013,vol. 15,p. 5602 - 5605.

29
[ 580-18-7 ]
[ 396-31-6 ]

References: [1]Organic Letters,2013,vol. 15,p. 5602 - 5605.

30
[ 5332-24-1 ]
[ 396-31-6 ]

References: [1]Journal of the American Chemical Society,2014,vol. 136,p. 3792 - 3795.

31
[ 396-31-6 ]
[ 2925-55-5 ]

Yield	Reaction Conditions	Operation in experiment
	With chlorosulfonic acid; at 130℃;	A mixture of <strong>[396-31-6]3-fluoroquinoline</strong> (0.6 g, 4.08 mmol) and HSO3CI (2 mL) in a round bottom flask equipped with a cooling condenser was stirred at 130C overnight. When TLC indicated that the reaction was complete, the resulting mixture was carefully poured into crushed ice, the mixture was extracted with DCM (100 mL x 3), and the combined organic layers were dried over Na2S04, and concentrated. The crude mixture was purified by chromatography (5% Ethyl Acetate/PE) to give the desired 3- fluoroquinoline-8-sulfonyl chloride. 1H NMR (CHLOROFORM-d) δ: 9.15 (d, J = 2.6 Hz, 1H), 8.53 (d, J = 7.6 Hz, 1H), 8.23 (dd, J = 8.2, 0.9 Hz, 1H), 7.97 (dd, J = 8.1, 2.8 Hz, 1H), 7.69 - 7.83 (m, 1H). LC-MS: m/z 246.7 (M+H)+
	With chlorosulfonic acid; at 130℃;	A mixture of <strong>[396-31-6]3-fluoroquinoline</strong> (0.6 g, 4.08 mmol) and HSO3Cl (2 mL) in a round bottom flask equipped with a cooling condenser was stirred at 130 C. overnight. When TLC indicated that the reaction was complete, the resulting mixture was carefully poured into crushed ice, the mixture was extracted with DCM (100 mL×3), and the combined organic layers were dried over Na2SO4, and concentrated. The crude mixture was purified by chromatography (5% Ethyl Acetate/PE) to give the desired <strong>[396-31-6]3-fluoroquinoline</strong>-8-sulfonyl chloride. 1H NMR (CHLOROFORM-d) δ: 9.15 (d, J=2.6 Hz, 1H), 8.53 (d, J=7.6 Hz, 1H), 8.23 (dd, J=8.2, 0.9 Hz, 1H), 7.97 (dd, J=8.1, 2.8 Hz, 1H), 7.69-7.83 (m, 1H). LC-MS: m/z 246.7 (M+H)+
	With chlorosulfonic acid; at 130℃;	A mixture of <strong>[396-31-6]3-fluoroquinoline</strong> (0.6 g, 4.08 mmol) and HSO3CI (2 mL) in a round bottom flask equipped with a cooling condenser was stirred at 130C overnight. When TLC indicated that the reaction was complete, the resulting mixture was carefully poured into crushed ice, the mixture was extracted with DCM (100 mL x 3), and the combined organic layers were dried over Na2S04, and concentrated. The crude mixture was purified by chromatography (5% Ethyl Acetate/PE) to give the desired 3- fluoroquinoline-8-sulfonyl chloride. 1H NMR (CHLOROFORM-d) δ: 9.15 (d, J = 2.6 Hz, 1H), 8.53 (d, J = 7.6 Hz, 1H), 8.23 (dd, J = 8.2, 0.9 Hz, 1H), 7.97 (dd, J = 8.1, 2.8 Hz, 1H), 7.69 - 7.83 (m, 1H). LC-MS: m/z 246.7 (M+H)+

References: [1]Patent: WO2014/139144,2014,A1 .Location in patent: Page/Page column 178; 179.
[2]Patent: US2014/288081,2014,A1 .Location in patent: Paragraph 0735; 0736.
[3]Patent: WO2014/139325,2014,A1 .Location in patent: Page/Page column 191; 192.

32
[ 396-31-6 ]
N<SUP>1</SUP>-(1-adamantylmethyl)-N<SUP>3</SUP>-(3-fluoroquinolin-4-yl)butane-1,3-diamine [ No CAS ]

References: [1]Journal of Medicinal Chemistry,2016,vol. 59,p. 264 - 281.

33
quinoline-3-diazonium tetrafluoroborate [ No CAS ]
[ 396-31-6 ]

References: [1]Angewandte Chemie - International Edition,2018,vol. 57,p. 9896 - 9900.
Angew. Chem.,2018,vol. 130,p. 10044 - 10048,5.

34
[ 396-31-6 ]
[ 407-25-0 ]
C₁₁H₉F₄NO [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
78%		General procedure: An oven-dried reaction vessel (4 or 9 ml screw-cap vial) equipped with a stirring bar was allowed to cool to room temperature under vacuum. Activated 4 A molecular sieves (crushed, 50 mg), [Rh-2 ] (and solid substrates, 1.0 equiv.), were added under air. The vial was then depressurized and pressurized with argon gas three times before the addition of dry THF (1 M) (and liquid substrates, distilled over CaH2, 1.0 equiv.). Following the addition of 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (2.0-4.0 equiv. as indicated), the glass vial was placed in a 150 ml stainless-steel autoclave under an argon atmosphere. The autoclave was pressurized and depressurized with hydrogen gas three times before the indicated pressure was set. The reaction mixture was stirred at 25-40 C for 24 h. After the autoclave was carefully depressurized, trifluoroacetic anhydride (3.0 equiv.) and CH2Cl2 (0.5 ml) were added to the crude mixture and stirring was continued for 10 min at room temperature. Alternatively, di-tert-butyl dicarbonate (3.0 equiv.), triethyl amine (3.0 equiv.) and CH2Cl2 (0.5 ml) were added to the reaction mixture and stirring was continued for 2 h at room temperature. The crude was then filtered over fritted funnel and the remaining solid was washed with ethyl acetate (2x 5 ml). The combined solution was concentrated under reduced pressure and submitted to column chromatography (pentane/ethyl acetate or pentane/dichloromethane) to obtain the final product. The indicated diastereoselectivities were determined by GC analysis or from the 19F NMR spectrum immediately after the reaction. NMR yield was calculated using hexafluorobenzene (20 μl, 0.173 mmol) as internal standard.

References: [1]Nature Chemistry,2019,vol. 11,p. 264 - 270.

35
[ 396-31-6 ]
[ 1309233-77-9 ]
[ 59321-69-6 ]

Yield	Reaction Conditions	Operation in experiment
83%	With palladium diacetate; 1-[2-(di-tert-butylphosphanyl)phenyl]-4-methoxy-piperidine; In tetrahydrofuran; toluene; at 110℃; for 12h;Inert atmosphere; Glovebox;	General procedure: In a glovebox, fluorinated benzoic acid (0.20 mmol),Pd(OAc)2 (2 mol%), and L5 (2 mol%) were charged to adried two-necked round-bottom reaction flask quippedwith an addition funnel, and ArTi(OiPr)3 (0.40 mmol) in1 cm3mixed solvents of toluene:THF (2:1) was added. Themixture was stirred at room temperature for 15 min andwarmed to 110 C and was allowed to react for 12 h andquenched with 10 cm3of water. The solution was extractedwith dichloromethane (3 × 30 cm3).The combined organicphase was dried over MgSO4and concentrated to drynessunder reduced pressure. The residue was purified by columnchromatography to give the coupling product.

References: [1]Monatshefte fur Chemie,2021,vol. 152,p. 823 - 832.

Historical Records

Technical Information

• Alkyl Halide Occurrence

Related Functional Groups of
[ 396-31-6 ]

Fluorinated Building Blocks

A104716 [851973-25-6]

3,6-Difluoroquinoline

Similarity: 1.00

A125471 [394-68-3]

8-Fluoroquinoline

Similarity: 0.97

A387388 [1781159-07-6]

3,8-Difluoroquinoline

Similarity: 0.97

A573340 [311346-65-3]

8-Fluoroquinoline hydrochloride

Similarity: 0.94

A543744 [145241-75-4]

6,8-Difluoroquinoline

Similarity: 0.94

Related Parent Nucleus of
[ 396-31-6 ]

Quinolines

A104716 [851973-25-6]

3,6-Difluoroquinoline

Similarity: 1.00

A125471 [394-68-3]

8-Fluoroquinoline

Similarity: 0.97

A387388 [1781159-07-6]

3,8-Difluoroquinoline

Similarity: 0.97

A573340 [311346-65-3]

8-Fluoroquinoline hydrochloride

Similarity: 0.94

A543744 [145241-75-4]

6,8-Difluoroquinoline

Similarity: 0.94

Precautionary Statements-General
Code	Phrase
P101	If medical advice is needed,have product container or label at hand.
P102	Keep out of reach of children.
P103	Read label before use
Prevention
Code	Phrase
P201	Obtain special instructions before use.
P202	Do not handle until all safety precautions have been read and understood.
P210	Keep away from heat/sparks/open flames/hot surfaces. - No smoking.
P211	Do not spray on an open flame or other ignition source.
P220	Keep/Store away from clothing/combustible materials.
P221	Take any precaution to avoid mixing with combustibles
P222	Do not allow contact with air.
P223	Keep away from any possible contact with water, because of violent reaction and possible flash fire.
P230	Keep wetted
P231	Handle under inert gas.
P232	Protect from moisture.
P233	Keep container tightly closed.
P234	Keep only in original container.
P235	Keep cool
P240	Ground/bond container and receiving equipment.
P241	Use explosion-proof electrical/ventilating/lighting/equipment.
P242	Use only non-sparking tools.
P243	Take precautionary measures against static discharge.
P244	Keep reduction valves free from grease and oil.
P250	Do not subject to grinding/shock/friction.
P251	Pressurized container: Do not pierce or burn, even after use.
P260	Do not breathe dust/fume/gas/mist/vapours/spray.
P261	Avoid breathing dust/fume/gas/mist/vapours/spray.
P262	Do not get in eyes, on skin, or on clothing.
P263	Avoid contact during pregnancy/while nursing.
P264	Wash hands thoroughly after handling.
P265	Wash skin thouroughly after handling.
P270	Do not eat, drink or smoke when using this product.
P271	Use only outdoors or in a well-ventilated area.
P272	Contaminated work clothing should not be allowed out of the workplace.
P273	Avoid release to the environment.
P280	Wear protective gloves/protective clothing/eye protection/face protection.
P281	Use personal protective equipment as required.
P282	Wear cold insulating gloves/face shield/eye protection.
P283	Wear fire/flame resistant/retardant clothing.
P284	Wear respiratory protection.
P285	In case of inadequate ventilation wear respiratory protection.
P231 + P232	Handle under inert gas. Protect from moisture.
P235 + P410	Keep cool. Protect from sunlight.
Response
Code	Phrase
P301	IF SWALLOWED:
P304	IF INHALED:
P305	IF IN EYES:
P306	IF ON CLOTHING:
P307	IF exposed:
P308	IF exposed or concerned:
P309	IF exposed or if you feel unwell:
P310	Immediately call a POISON CENTER or doctor/physician.
P311	Call a POISON CENTER or doctor/physician.
P312	Call a POISON CENTER or doctor/physician if you feel unwell.
P313	Get medical advice/attention.
P314	Get medical advice/attention if you feel unwell.
P315	Get immediate medical advice/attention.
P320
P302 + P352	IF ON SKIN: wash with plenty of soap and water.
P321
P322
P330	Rinse mouth.
P331	Do NOT induce vomiting.
P332	IF SKIN irritation occurs:
P333	If skin irritation or rash occurs:
P334	Immerse in cool water/wrap n wet bandages.
P335	Brush off loose particles from skin.
P336	Thaw frosted parts with lukewarm water. Do not rub affected area.
P337	If eye irritation persists:
P338	Remove contact lenses, if present and easy to do. Continue rinsing.
P340	Remove victim to fresh air and keep at rest in a position comfortable for breathing.
P341	If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing.
P342	If experiencing respiratory symptoms:
P350	Gently wash with plenty of soap and water.
P351	Rinse cautiously with water for several minutes.
P352	Wash with plenty of soap and water.
P353	Rinse skin with water/shower.
P360	Rinse immediately contaminated clothing and skin with plenty of water before removing clothes.
P361	Remove/Take off immediately all contaminated clothing.
P362	Take off contaminated clothing and wash before reuse.
P363	Wash contaminated clothing before reuse.
P370	In case of fire:
P371	In case of major fire and large quantities:
P372	Explosion risk in case of fire.
P373	DO NOT fight fire when fire reaches explosives.
P374	Fight fire with normal precautions from a reasonable distance.
P376	Stop leak if safe to do so. Oxidising gases (section 2.4) 1
P377	Leaking gas fire: Do not extinguish, unless leak can be stopped safely.
P378
P380	Evacuate area.
P381	Eliminate all ignition sources if safe to do so.
P390	Absorb spillage to prevent material damage.
P391	Collect spillage. Hazardous to the aquatic environment
P301 + P310	IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.
P301 + P312	IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P301 + P330 + P331	IF SWALLOWED: Rinse mouth. Do NOT induce vomiting.
P302 + P334	IF ON SKIN: Immerse in cool water/wrap in wet bandages.
P302 + P350	IF ON SKIN: Gently wash with plenty of soap and water.
P303 + P361 + P353	IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.
P304 + P312	IF INHALED: Call a POISON CENTER or doctor/physician if you feel unwell.
P304 + P340	IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.
P304 + P341	IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing.
P305 + P351 + P338	IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.
P306 + P360	IF ON CLOTHING: Rinse Immediately contaminated CLOTHING and SKIN with plenty of water before removing clothes.
P307 + P311	IF exposed: call a POISON CENTER or doctor/physician.
P308 + P313	IF exposed or concerned: Get medical advice/attention.
P309 + P311	IF exposed or if you feel unwell: call a POISON CENTER or doctor/physician.
P332 + P313	IF SKIN irritation occurs: Get medical advice/attention.
P333 + P313	IF SKIN irritation or rash occurs: Get medical advice/attention.
P335 + P334	Brush off loose particles from skin. Immerse in cool water/wrap in wet bandages.
P337 + P313	IF eye irritation persists: Get medical advice/attention.
P342 + P311	IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician.
P370 + P376	In case of fire: Stop leak if safe to Do so.
P370 + P378	In case of fire:
P370 + P380	In case of fire: Evacuate area.
P370 + P380 + P375	In case of fire: Evacuate area. Fight fire remotely due to the risk of explosion.
P371 + P380 + P375	In case of major fire and large quantities: Evacuate area. Fight fire remotely due to the risk of explosion.
Storage
Code	Phrase
P401
P402	Store in a dry place.
P403	Store in a well-ventilated place.
P404	Store in a closed container.
P405	Store locked up.
P406	Store in corrosive resistant/ container with a resistant inner liner.
P407	Maintain air gap between stacks/pallets.
P410	Protect from sunlight.
P411
P412	Do not expose to temperatures exceeding 50 oC/ 122 oF.
P413
P420	Store away from other materials.
P422
P402 + P404	Store in a dry place. Store in a closed container.
P403 + P233	Store in a well-ventilated place. Keep container tightly closed.
P403 + P235	Store in a well-ventilated place. Keep cool.
P410 + P403	Protect from sunlight. Store in a well-ventilated place.
P410 + P412	Protect from sunlight. Do not expose to temperatures exceeding 50 oC/122oF.
P411 + P235	Keep cool.
Disposal
Code	Phrase
P501	Dispose of contents/container to ...
P502	Refer to manufacturer/supplier for information on recovery/recycling

Physical hazards
Code	Phrase
H200	Unstable explosive
H201	Explosive; mass explosion hazard
H202	Explosive; severe projection hazard
H203	Explosive; fire, blast or projection hazard
H204	Fire or projection hazard
H205	May mass explode in fire
H220	Extremely flammable gas
H221	Flammable gas
H222	Extremely flammable aerosol
H223	Flammable aerosol
H224	Extremely flammable liquid and vapour
H225	Highly flammable liquid and vapour
H226	Flammable liquid and vapour
H227	Combustible liquid
H228	Flammable solid
H229	Pressurized container: may burst if heated
H230	May react explosively even in the absence of air
H231	May react explosively even in the absence of air at elevated pressure and/or temperature
H240	Heating may cause an explosion
H241	Heating may cause a fire or explosion
H242	Heating may cause a fire
H250	Catches fire spontaneously if exposed to air
H251	Self-heating; may catch fire
H252	Self-heating in large quantities; may catch fire
H260	In contact with water releases flammable gases which may ignite spontaneously
H261	In contact with water releases flammable gas
H270	May cause or intensify fire; oxidizer
H271	May cause fire or explosion; strong oxidizer
H272	May intensify fire; oxidizer
H280	Contains gas under pressure; may explode if heated
H281	Contains refrigerated gas; may cause cryogenic burns or injury
H290	May be corrosive to metals
Health hazards
Code	Phrase
H300	Fatal if swallowed
H301	Toxic if swallowed
H302	Harmful if swallowed
H303	May be harmful if swallowed
H304	May be fatal if swallowed and enters airways
H305	May be harmful if swallowed and enters airways
H310	Fatal in contact with skin
H311	Toxic in contact with skin
H312	Harmful in contact with skin
H313	May be harmful in contact with skin
H314	Causes severe skin burns and eye damage
H315	Causes skin irritation
H316	Causes mild skin irritation
H317	May cause an allergic skin reaction
H318	Causes serious eye damage
H319	Causes serious eye irritation
H320	Causes eye irritation
H330	Fatal if inhaled
H331	Toxic if inhaled
H332	Harmful if inhaled
H333	May be harmful if inhaled
H334	May cause allergy or asthma symptoms or breathing difficulties if inhaled
H335	May cause respiratory irritation
H336	May cause drowsiness or dizziness
H340	May cause genetic defects
H341	Suspected of causing genetic defects
H350	May cause cancer
H351	Suspected of causing cancer
H360	May damage fertility or the unborn child
H361	Suspected of damaging fertility or the unborn child
H361d	Suspected of damaging the unborn child
H362	May cause harm to breast-fed children
H370	Causes damage to organs
H371	May cause damage to organs
H372	Causes damage to organs through prolonged or repeated exposure
H373	May cause damage to organs through prolonged or repeated exposure
Environmental hazards
Code	Phrase
H400	Very toxic to aquatic life
H401	Toxic to aquatic life
H402	Harmful to aquatic life
H410	Very toxic to aquatic life with long-lasting effects
H411	Toxic to aquatic life with long-lasting effects
H412	Harmful to aquatic life with long-lasting effects
H413	May cause long-lasting harmful effects to aquatic life
H420	Harms public health and the environment by destroying ozone in the upper atmosphere

{[proInfo.proName]}

CAS No.: 396-31-6

{[proInfo.proName]}