1455091-10-7|Methyl 4-hydroxy-7-phenoxyisoquinoline-3-carboxylate| Ambeed

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Quality Control of [ 1455091-10-7 ] Purity: 97% SDS Specification

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Product Details of [ 1455091-10-7 ]

CAS No. :	1455091-10-7
Formula :	C₁₇H₁₃NO₄
M.W :	295.29
SMILES Code :	O=C(C1=C(O)C2=C(C=N1)C=C(OC3=CC=CC=C3)C=C2)OC
MDL No. :	MFCD29075436
InChI Key :	YTWDBRIDKWWANA-UHFFFAOYSA-N
Pubchem ID :	86709142

Safety of [ 1455091-10-7 ]

GHS Pictogram:
Signal Word:	Warning
Hazard Statements:	H302-H315-H319-H335
Precautionary Statements:	P261-P305+P351+P338

Computational Chemistry of [ 1455091-10-7 ] Show Less

Physicochemical Properties

Num. heavy atoms	22
Num. arom. heavy atoms	16
Fraction Csp3	0.06
Num. rotatable bonds	4
Num. H-bond acceptors	5.0
Num. H-bond donors	1.0
Molar Refractivity	81.56
TPSA ? Topological Polar Surface Area: Calculated from Ertl P. et al. 2000 J. Med. Chem.	68.65 Å²

Lipophilicity

Log P_o/w (iLOGP)? iLOGP: in-house physics-based method implemented from Daina A et al. 2014 J. Chem. Inf. Model.	2.48
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	4.01
Log P_o/w (WLOGP)? WLOGP: Atomistic method implemented from Wildman SA and Crippen GM. 1999 J. Chem. Inf. Model.	3.52
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.	1.82
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	2.95
Consensus Log P_o/w? Consensus Log P_o/w: Average of all five predictions	2.96

Water Solubility

Log S (ESOL):? ESOL: Topological method implemented from Delaney JS. 2004 J. Chem. Inf. Model.	-4.47
Solubility	0.00998 mg/ml ; 0.0000338 mol/l
Class? Solubility class: Log S scale Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly	Moderately soluble
Log S (Ali)? Ali: Topological method implemented from Ali J. et al. 2012 J. Chem. Inf. Model.	-5.15
Solubility	0.00207 mg/ml ; 0.00000701 mol/l
Class? Solubility class: Log S scale Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly	Moderately 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	-5.45
Solubility	0.00105 mg/ml ; 0.00000354 mol/l
Class? Solubility class: Log S scale Insoluble < -10 < Poorly < -6 < Moderately < -4 < Soluble < -2 Very < 0 < Highly	Moderately 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	Yes
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	Yes
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	Yes
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.	-5.25 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	0.0
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)	2.21

Application In Synthesis of [ 1455091-10-7 ]

* 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 [ 1455091-10-7 ]

[ 1455091-10-7 ] Synthesis Path-Downstream 1~35

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[ 1455091-04-9 ]
[ 1455091-10-7 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 59193-77-0 ]
[ 1455091-10-7 ]
[ 1455094-69-5 ]

Yield	Reaction Conditions	Operation in experiment
300 mg	In ethanol; for 18h;Reflux;	To a solution of the 3-amino-2,2-dimethyl-propionic acid ethyl ester (598 mg, 4.12 mmol) in EtOH (9.1 mL) at r.t. were added 4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid methyl ester (81 1 mg, 2.75 mmol) to give suspension solution, the reaction mixture was allowed to reflux for 18 h. After cooled to rt, the solvent was evaporated in vacuo, the crude was purified by silica gel chromatography to give 300 mg of title compound as a yellow oil: MS (m/z) 409.0 (M+l)+.

References: [1]Patent: WO2013/134660,2013,A1 .Location in patent: Paragraph 0493.

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[ 1455091-06-1 ]
[ 1455091-10-7 ]

Yield	Reaction Conditions	Operation in experiment
78.8%	With sodium methylate; In methanol; dimethyl sulfoxide; at 20℃; for 2h;	Ice bath,Sodium methoxide (12.70 g 2.34.60 mmol)Of methanol (40 mL)The solution was added dropwise to a solution of methyl 2 - (((N- (2-methoxy-2-oxoethyl) -4-methylphenyl) sulfonyl) methyl) -4-phenoxybenzoate 18.90 g, 39.10 mmol)In dimethyl sulfoxide (82 mL), after completion of the dropwise addition,The reaction solution was stirred at room temperature for 2 hours.The methanol was removed under reduced pressure,Add water (50 mL) dilute the concentrate,The pH was adjusted to pH = 10 with 1N dilute hydrochloric acid.Ethyl acetate (100 mL x 3)The organic layer was washed with water (100 mL) and saturated brine (100 mL), respectively,Dried over anhydrous sodium sulfate. Concentrated under reduced pressure,The concentrate was subjected to column separation to give 9.1 g of a white solid in a yield of 78.8%.
72.9%	With sodium methylate; In methanol; dimethyl sulfoxide; at 20℃; for 0.5h;	To a mixture of 2- [Methoxycarbonylmethyl-(toluene-4-sulfonyl)-amino]-methyl}-4- phenoxy-benzoic acid methyl ester (14.0 g, 28.1 mmol) in DMSO (56 mL) was slowly added 30% NaOMe in MeOH (15.3 mL, 84.3 mmol). The resultant mixture was stirred at room temperature for 30 min and poured into 200 mL of ice and water. It was slowly acidified by cone. HCl aq. solution (10 mL) and then extracted with EtOAc. Organic layer was washed with 3% NaHC03 solution, water and brine, and was dried over Na2SO/t, filtered and concentrated. Crude produce was purified by silica gel chromatography to provide the title compound 6.05 g (20.5 mmol) in 72.9% yield. lH NMR in CDCI3, delta in ppm: 1 1.7 (s, 1 H), 8.59 (s, 1 H), 8.36 (d, 1 H, J = 9.2 Hz), 7.55-7.1 (m, 7 H), 4.07 (s, 3 H).

References: [1]Patent: CN106083720,2016,A .Location in patent: Paragraph 0062; 0071-0072.
[2]Patent: WO2013/134660,2013,A1 .Location in patent: Paragraph 0169.

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[ 1455091-10-7 ]
[ 1421312-34-6 ]

References: [1]Patent: WO2013/134660,2013,A1 .
[2]Patent: WO2014/14834,2014,A1 .
[3]Patent: CN106083720,2016,A .
[4]Patent: CN108341777,2018,A .
[5]Patent: CN108341777,2018,A .
[6]Patent: CN109956901,2019,A .
[7]Patent: CN110903242,2020,A .

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[ 1455091-10-7 ]
[ 1455089-22-1 ]

References: [1]Patent: WO2013/134660,2013,A1 .

6
[ 1455091-10-7 ]
[ 1455087-02-1 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455091-10-7 ]
[ 1455094-16-2 ]

References: [1]Patent: WO2013/134660,2013,A1 .

8
[ 1455091-10-7 ]
[ 1455089-85-6 ]

References: [1]Patent: WO2013/134660,2013,A1 .

9
[ 1455091-10-7 ]
[ 1455091-21-0 ]

Yield	Reaction Conditions	Operation in experiment
90.7%	With N-Bromosuccinimide; In dichloromethane; for 2h;	Add dichloromethane (2L) and <strong>[1455091-10-7]4-hydroxy-7-phenoxyisoquinoline-3-carboxylic acid methyl ester</strong> (200.00g, 0.68mol) to the reaction flask in sequence, after stirring,Add N-bromosuccinimide (NBS) (126.60g, 0.71mol) into the reaction bottle, and after the end of the addition, react for 2 hours.After distilling off about half of the methylene chloride under reduced pressure, methanol (2L) was added, and the crystal was stirred for 1h.After filtration, the filter cake was blow-dried to obtain 1-bromo-<strong>[1455091-10-7]4-hydroxy-7-phenoxyisoquinoline-3-carboxylic acid methyl ester</strong> (229.67g, yield 90.7%, purity 98.98%).
86.4%	With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; In methanol; at 5℃;Reflux;	Methyl 4-hydroxy-7-phenoxyisoquinoline-3-carboxylate (Compound A) 2.95 g,The stirring temperature of the ice water bath was lowered to 5-10 C, and 1.57 g of 1,3-dibromo-5,5-dimethylhydantoin was added, and methanol was used as a solvent, and the reaction was refluxed for 4-6 h.The TLC monitors the reaction to the starting material completely, 0~10 C, suction filtration, the filter cake is rinsed with methanol, and dried under vacuum.A pale yellow solid, Compound B (yield 86.4%, purity 98.5%) was obtained.
58%	With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; for 1h;Reflux;	A mixture of 4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid methyl ester (6.0 g, 20.32 mmol), N-bromosuccinimide (3.80 g, 21.33 mmol) and benzoyl peroxide (246 mg, 1.01 mmol) in CCI4 was refluxed for 1 h. Solid was filtered off through a plug of silica gel. Filtrate was concentrated and purified by silica chromatography, eluting with EtOAc. All fractions contain the desired product was combined and concentrated. Residue was suspended in 150 mL of (3/1) MeOH/EtOAc and was refluxed for 1 h. After cooled, solid was collected, rinsed with MeOH and dried on vacuo to provide the title compound 4.42 g (1 1.8 mmol) in 58% yield as a white solid. H NMR in CDC13, delta ppm: 1 1.7 (s, 1 H), 8.36 (d, 1 H, J = 9.2 Hz), 7.63 (d, 1 H, J = 2.4 Hz), 7.55-7.10 (m, 6 H), 4.06 (s, 3 H).

References: [1]Patent: CN110903242,2020,A .Location in patent: Paragraph 0065-0069.
[2]Patent: CN109956901,2019,A .Location in patent: Paragraph 0055-0058.
[3]Patent: WO2013/134660,2013,A1 .Location in patent: Paragraph 0183.

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[ 1455094-35-5 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455090-01-3 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455090-03-5 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455094-37-7 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455090-05-7 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455090-10-4 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455094-71-9 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455094-73-1 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455091-10-7 ]
[ 1455094-75-3 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455091-10-7 ]
[ 1455090-30-8 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455091-10-7 ]
[ 1455094-78-6 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455091-10-7 ]
[ 1455094-80-0 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455094-82-2 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455091-10-7 ]
[ 1455094-84-4 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455091-10-7 ]
[ 1455090-32-0 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455091-10-7 ]
[ 1455087-12-3 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455091-10-7 ]
[ 1455087-16-7 ]

References: [1]Patent: WO2013/134660,2013,A1 .

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[ 1455091-10-7 ]
[ 107-95-9 ]
[ 1455086-85-7 ]

Yield	Reaction Conditions	Operation in experiment
89%	With sodium methylate; In methanol;Reflux;	A mixture of 4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid methyl ester (185 mg, 0.55 mmol), beta-alanine (489 mg, 5.5 mmol) in 0.5 M NaOMe in MeOH solution (8.8 mL, 4.4 mmol) was refluxed overnight. After cooled, the reaction mixture was concentrated and residue was dissolved in water (80 mL). It was acidified by 1 N HC1 solution to pH ca. 3-4. Resulting gummy solid was collected by filtration, rinsed with water and then dissolved in EtOAc. The organic solution was dried over MgSO/t, filtered and concentrated to provide the title compound (173 mg, 0.49 mmol) as an off-white solid in 89% yield. LC-MS ESI-: 351.14 (M-l)

References: [1]Patent: WO2013/134660,2013,A1 .Location in patent: Paragraph 0170.

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[ 19036-43-2 ]
[ 1455091-10-7 ]
[ 1455086-87-9 ]

Yield	Reaction Conditions	Operation in experiment
81%	With sodium methylate; In methanol; at 120℃; for 1h;Microwave irradiation;	A mixture of 4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid methyl ester (68 mg, 0.23 mmol) and 3-amino-2,2-dimethyl-propionic acid (81 mg, 0.69 mmol) (ChemBridge) in 0.5 N NaOMe in MeOH solution (0.92 mL, 0.46 mmol) was microwaved at 120 C for 1 h. Reaction mixture was diluted with water (50 mL) and acidified by 1 N HC1 solution to pH = 3-4. Precipitate was collected and rinsed with water and dried in vacuo to provide the title compound (71 mg, 0.19 mmol) as an off- white solid in 81% yield. LC-MS ESI-: 379.04 (M-l)

References: [1]Patent: WO2013/134660,2013,A1 .Location in patent: Paragraph 0171.

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[ 565-71-9 ]
[ 1455091-10-7 ]
[ 1455086-89-1 ]

Yield	Reaction Conditions	Operation in experiment
92%	With sodium methylate; In methanol; at 120℃; for 1h;Microwave irradiation;	A mixture of 4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid methyl ester(90 mg, 0.31 mmol) and 2-(S)-hydroxy-3-amino-propionic acid (Sigma-Aldrich) (96 mg, 0.92 mmol) in 0.5 N NaOMe in MeOH solution (1.22 mL, 0.61 mmol) was microwaved at 120 °C for 1 h and concentrated. Residue was dissolved in water (70 mL) and acidified by 1 N HC1 solution to pH = 3-4. It was extracted with EtOAc, Organic layer was washed with brine, dried over MgSO/t, filtered and concentrated to give the title compound (105 mg, 0.29 mmol) in 92percent yield. LC-MS ESI-: 366.99 (M- 1)-.

References: [1]Patent: WO2013/134660,2013,A1 .Location in patent: Paragraph 0172.

30
[ 1455091-10-7 ]
[ 56-12-2 ]
[ 1455086-92-6 ]

Yield	Reaction Conditions	Operation in experiment
94%	With sodium methylate; In methanol;Reflux;	A mixture of 4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid methyl ester (100 mg, 0.34 mmol) and 4-aminobutyric acid (525 mg, 5.1 mmol) in 0.5 N NaOMe in MeOH solution (6.8 mL, 3.4 mmol) was heated to reflux overnight. Reaction mixture was diluted with water (100 mL) and acidified by 1 N HC1 solution to pH = 3-4. Precipitate was collected and rinsed with water. It was dried in vacuo to provide the title compound (117 mg, 0.32mmol) in 94% yield. LC-MS ESI-: 365.05 (M-l)

References: [1]Patent: WO2013/134660,2013,A1 .Location in patent: Paragraph 0173.

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[ 1455091-10-7 ]
[ 660-88-8 ]
[ 1455086-94-8 ]

Yield	Reaction Conditions	Operation in experiment
80%	With sodium methylate; In methanol;Reflux;	A mixture of 4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid methyl ester (100 mg, 0.34 mmol) and 5-amino-valeric acid (597 mg, 5.1 mmol) in 0.5 N NaOMe in MeOH solution (6.8 mL, 3.4 mmol) was heated to reflux overnight. Reaction mixture was diluted with water (100 mL) and acidified by 1 N HC1 solution to pH = 3-4. Precipitate was collected and rinsed with water. It was dried in vacuo to provide the title compound (102 mg, 0.27mmol) in 80% yield. LC-MS ESI-: 379.07 (M-l)

References: [1]Patent: WO2013/134660,2013,A1 .Location in patent: Paragraph 0174.

32
[ 625-05-8 ]
[ 1455091-10-7 ]
[ 1455086-95-9 ]

Yield	Reaction Conditions	Operation in experiment
33%	With sodium methylate; In N,N-dimethyl-formamide; for 2h;Reflux;	To a mixture of 4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid methyl ester (100 mg, 0.34 mmol) and 3-amino-3-methyl-butyric acid (Oakwood) (199 mg, 1.7 mmol) in DMF (3 mL) was added sodium methoxide solid (73 mg, 1.36 mmoL). The mixture was gently refluxed for 2 h. After cooled, it was diluted with water (100 mL) and acidified by 1 N HC1 aqueous solution to pH = 3-4. Precipitate was collected and dried in vacuo. The crude product was purified by silica gel chromatography, eluting with 20percent - 100percent EtOAc-hexanes, to provide the title compound (42 mg, 0.1 1 mmol) in 33percent yield. LC-MS ESI-: 379.04 (M-l)\

References: [1]Patent: WO2013/134660,2013,A1 .Location in patent: Paragraph 0175.

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[ 3938-83-8 ]
[ 1455091-10-7 ]
[ 1455086-97-1 ]

Yield	Reaction Conditions	Operation in experiment
92.4%	With sodium methylate; In methanol; at 120℃; for 1h;Microwave irradiation;	A mixture of 4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid methyl ester (100 mg, 0.34 mmol) and (S)-(-)-4-amino-2-hydroxybutyric acid (122 mg, 1.02 mmol) in 0.5 N NaOMe in MeOH solution (1.4 mL, 0.7 mmol) was microwaved at 120 C for 1 h. Reaction mixture was diluted with water (100 mL), acidified by 1 N HC1 aqueous solution to pH = 3-4 and extracted with EtOAc. Organic layer was washed with brine, dried over Mg2S04, filtered and concentrated to provide the title compound (120 mg, 0.31mmol) in 92.4 % yield. LC-MS ESI-: 381.05 (M-l)

References: [1]Patent: WO2013/134660,2013,A1 .Location in patent: Paragraph 0176.

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[ 1455091-10-7 ]
[ 1455091-14-1 ]
[ 1455091-17-4 ]

Yield	Reaction Conditions	Operation in experiment
23.6%	With sodium methylate; In methanol; at 130℃; for 3h;Microwave irradiation;	A mixture of 4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid methyl ester (80 mg, 0.27mmol) and 4-amino-2,2-dimethyl-butyric acid methyl ester, trifluoroacetic acid salt (210 mg, 0.81mmol) in 0.5 M NaOMe/MeOH solution (1.62 mL, 0.81 mmol) was microwaved at 130 C for 3 h. The reaction mixture was diluted with water (50 mL), acidified by 1 N HC1 to pH = 3-4 and then extracted with EtOAc. Organic layer was washed with water, brine, dried over MgS04, filtered and concentrated. Residue was purified by silica gel chromatography, eluting with 5 - 50% EtOAc/hexanes, to provide the title compound 26 mg (0.063 mmol) in 23.6% yield. lH NMR in CDCI3, delta ppm: 13.23 (s, 1 H), 8.40 (s, 1 H), 8.32 (d, J = 8.8 Hz, 1 H), 7.97 (br t, 1 H), 7.42 (m, 4 H), 7.12 (m, 3 H), 3.64 (s, 3 H), 3.52 (m, 2 H), 1.95 (dd, J = 9.1, 5.9 Hz, 2 H), 1.27 (s, 6 H).

References: [1]Patent: WO2013/134660,2013,A1 .Location in patent: Paragraph 0179.

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[ 1455091-10-7 ]
[ 76387-70-7 ]
[ 1455091-19-6 ]

Yield	Reaction Conditions	Operation in experiment
88%	With sodium methylate; In methanol; for 30h;Reflux;	A mixture of 4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid methyl ester (100 mg, 0.34 mmol) and 3-(S)-amino-2-tert-butoxycarbonylamino-propionic acid (346 mg, 1.69 mmol) (Bachem Americas, Torrance CA) in 0.5 M NaOMe/MeOH solution (2.7 mL, 1.36 mmol) was refluxed for 30 h. It was diluted with water (75 mL), acidified by 1 N HCl to pH = 5. Precipitate was collected, rinsed with water and dried in vacuo to provide the title compound 140 mg (0.30 mmol) in 88% yield. LC-MS ESI-: 466.10 (M- l)

References: [1]Patent: WO2013/134660,2013,A1 .Location in patent: Paragraph 0181.

Historical Records

Technical Information

• Acyl Group Substitution • Appel Reaction • Bouveault-Blanc Reduction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Catalytic Hydrogenation • Chugaev Reaction • Complex Metal Hydride Reductions • Corey-Kim Oxidation • Dess-Martin Oxidation • Ester Cleavage • Hydride Reductions • Jones Oxidation • Martin's Sulfurane Dehydrating Reagent • Mitsunobu Reaction • Moffatt Oxidation • Nomenclature of Ethers • Oxidation of Alcohols by DMSO • Preparation of Alcohols • Preparation of Amines • Preparation of Ethers • Reactions of Alcohols • Reactions of Benzene and Substituted Benzenes • Reactions of Ethers • Reactions with Organometallic Reagents • Ritter Reaction • Sharpless Olefin Synthesis • Specialized Acylation Reagents-Carbodiimides and Related Reagents • Swern Oxidation

Related Functional Groups of
[ 1455091-10-7 ]

Aryls

A294838 [18735-74-5]

5-Methyl-2-phenyloxazole-4-carboxylic acid

Similarity: 0.77

A483398 [99924-18-2]

5-Phenyloxazole-4-carboxylic acid

Similarity: 0.73

A180699 [13676-47-6]

2-(4-Aminophenyl)benzo[d]oxazol-5-amine

Similarity: 0.68

A292265 [1367920-70-4]

(2-Phenylbenzo[d]oxazol-6-yl)methanamine

Similarity: 0.67

A302905 [51362-40-4]

6-Phenoxypicolinic acid

Similarity: 0.66

Ethers

A211696 [27568-04-3]

Ethyl 4-hydroxy-8-methoxyquinoline-3-carboxylate

Similarity: 0.71

A490705 [14446-31-2]

6-Methoxy-3-methylisoquinoline

Similarity: 0.67

A118044 [28027-17-0]

4-Hydroxy-7-methoxyquinoline-3-carboxylic acid

Similarity: 0.66

A181855 [28027-16-9]

4-Hydroxy-6-methoxyquinoline-3-carboxylic acid

Similarity: 0.66

A302905 [51362-40-4]

6-Phenoxypicolinic acid

Similarity: 0.66

Alcohols

A211696 [27568-04-3]

Ethyl 4-hydroxy-8-methoxyquinoline-3-carboxylate

Similarity: 0.71

A181855 [28027-16-9]

4-Hydroxy-6-methoxyquinoline-3-carboxylic acid

Similarity: 0.66

A571882 [65-22-5]

3-Hydroxy-5-(hydroxymethyl)-2-methylisonicotinaldehyde hydrochloride

Similarity: 0.66

A153405 [58481-17-7]

Methyl 2-(hydroxymethyl)isonicotinate

Similarity: 0.66

A273835 [90800-42-3]

8-Hydroxyquinoline-6-carboxylic acid

Similarity: 0.64

Esters

A284741 [27104-73-0]

Methyl isoquinoline-3-carboxylate

Similarity: 0.76

A108949 [50458-79-2]

Ethyl 3-isoquinolinecarboxylate

Similarity: 0.74

A100218 [882679-56-3]

Ethyl 6-bromoisoquinoline-3-carboxylate

Similarity: 0.72

A375605 [660830-62-6]

Ethyl 7-bromoisoquinoline-3-carboxylate

Similarity: 0.72

A211696 [27568-04-3]

Ethyl 4-hydroxy-8-methoxyquinoline-3-carboxylate

Similarity: 0.71

Related Parent Nucleus of
[ 1455091-10-7 ]

Isoquinolines

A284741 [27104-73-0]

Methyl isoquinoline-3-carboxylate

Similarity: 0.76

A108949 [50458-79-2]

Ethyl 3-isoquinolinecarboxylate

Similarity: 0.74

A100218 [882679-56-3]

Ethyl 6-bromoisoquinoline-3-carboxylate

Similarity: 0.72

A375605 [660830-62-6]

Ethyl 7-bromoisoquinoline-3-carboxylate

Similarity: 0.72

A205967 [203626-75-9]

Isoquinoline-3-carboxylic acid hydrate

Similarity: 0.69

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

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CAS No.: 1455091-10-7

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CAS No.: 1455091-10-7

Alternative Products

Product Details of [ 1455091-10-7 ]

Safety of [ 1455091-10-7 ]

Computational Chemistry of [ 1455091-10-7 ] Show Less

Physicochemical Properties

Lipophilicity

Water Solubility

Pharmacokinetics

Druglikeness

Medicinal Chemistry

Application In Synthesis of [ 1455091-10-7 ]

[ 1455091-10-7 ] Synthesis Path-Downstream 1~35

Related Products

Historical Records

Technical Information

Categories

Related Functional Groups of
[ 1455091-10-7 ]

Aryls

Ethers

Alcohols

Esters

Related Parent Nucleus of
[ 1455091-10-7 ]

Isoquinolines

Precautionary Statements-General

Prevention

Response

Storage

Disposal

Physical hazards

Health hazards

Environmental hazards

Inquiry

Molarity Calculator

Total Compounds Calculator

Dissolution Calculator

{[proInfo.proName]}

CAS No.: 1455091-10-7

{[proInfo.proName]}

CAS No.: 1455091-10-7

Alternative Products

Product Details of [ 1455091-10-7 ]

Safety of [ 1455091-10-7 ]

Computational Chemistry of [ 1455091-10-7 ] Show Less

Physicochemical Properties

Lipophilicity

Water Solubility

Pharmacokinetics

Druglikeness

Medicinal Chemistry

Application In Synthesis of [ 1455091-10-7 ]

[ 1455091-10-7 ] Synthesis Path-Downstream 1~35

Related Products

Historical Records

Technical Information

Categories

Related Functional Groups of [ 1455091-10-7 ]

Aryls

Ethers

Alcohols

Esters

Related Parent Nucleus of [ 1455091-10-7 ]

Isoquinolines

Precautionary Statements-General

Prevention

Response

Storage

Disposal

Physical hazards

Health hazards

Environmental hazards

Inquiry

Molarity Calculator

Total Compounds Calculator

Dissolution Calculator

Related Functional Groups of
[ 1455091-10-7 ]

Related Parent Nucleus of
[ 1455091-10-7 ]