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[ CAS No. 165454-18-2 ] {[proInfo.proName]}

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Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
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3d Animation Molecule Structure of 165454-18-2
Chemical Structure| 165454-18-2
Chemical Structure| 165454-18-2
Structure of 165454-18-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 165454-18-2 ]

CAS No. :165454-18-2 MDL No. :MFCD18818656
Formula : C6H13NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :VMVFDJKCPYECQV-UHFFFAOYSA-N
M.W : 131.17 Pubchem ID :45087481
Synonyms :

Calculated chemistry of [ 165454-18-2 ]

Physicochemical Properties

Num. heavy atoms : 9
Num. arom. heavy atoms : 0
Fraction Csp3 : 1.0
Num. rotatable bonds : 2
Num. H-bond acceptors : 3.0
Num. H-bond donors : 1.0
Molar Refractivity : 34.02
TPSA : 32.7 Ų

Pharmacokinetics

GI absorption : High
BBB permeant : No
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -7.75 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.58
Log Po/w (XLOGP3) : -0.91
Log Po/w (WLOGP) : -0.69
Log Po/w (MLOGP) : -0.67
Log Po/w (SILICOS-IT) : 0.17
Consensus Log Po/w : -0.1

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : 0.05
Solubility : 148.0 mg/ml ; 1.13 mol/l
Class : Highly soluble
Log S (Ali) : 0.71
Solubility : 667.0 mg/ml ; 5.09 mol/l
Class : Highly soluble
Log S (SILICOS-IT) : -0.34
Solubility : 59.4 mg/ml ; 0.453 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 0.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.28

Safety of [ 165454-18-2 ]

Signal Word:Danger Class:8
Precautionary Statements:P210-P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P310-P330-P332+P313-P362-P370+P378-P403+P233-P403+P235-P405-P501 UN#:3259
Hazard Statements:H302-H315-H318-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 165454-18-2 ]

* 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 [ 165454-18-2 ]

[ 165454-18-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2838104-84-8 ]
  • [ 165454-18-2 ]
  • [ 2838105-43-2 ]
YieldReaction ConditionsOperation in experiment
155 mg Stage #1: (3-(dimethylamine)oxetan-3-yl)methanol With sodium hydride In tetrahydrofuran at 0℃; Stage #2: 7-bromo-5-fluoro-N-(5-fluoroquinolin-6-yl)quinazolin-4-amine In tetrahydrofuran at 25 - 80℃; 21.1 Step 1: 7-bromo-5-((3-(dimethylamino)oxetan-3-yl)methoxy)-N-(5-fluoroquinolin-6- yl)quinazolin-4-amine To a solution of (3-(dimethylamine) oxetan-3-yl)methanol (67.6 mg, 516 µmol,1 eq) in THF (5 ml). was added NaH (18.5 mg, 774 µmol) at 0°C, the reaction mixture was stirred at 0 °C for 15 min, then Intermediate 2 (100 mg, 258 µmol) was added to the reaction mixture at 25 °C, the resulting solution was stirred for 4 hours at 80°C. Then it was cooled to room temperature. The resulting solution was diluted with 20 mL of water. The resulting solution was extracted with 2x20 mL of ethyl acetate, the organic layers combined, and the resulting mixture was washed with 20 mL of brine. The mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. The product was purified by chromatography with DCM: MeOH to afford the title compound (120 mg, yield:93.7 %) as a yellow solid. LC-MS: (ES, m/z): RT = 1.037 min, LCMS: m/z = 498 [M+1].
155 mg Stage #1: (3-(dimethylamine)oxetan-3-yl)methanol With sodium hydride In tetrahydrofuran at 0℃; Stage #2: 7-bromo-5-fluoro-N-(5-fluoroquinolin-6-yl)quinazolin-4-amine In tetrahydrofuran at 25 - 80℃; 21.1 Step 1: 7-bromo-5-((3-(dimethylamino)oxetan-3-yl)methoxy)-N-(5-fluoroquinolin-6- yl)quinazolin-4-amine To a solution of (3-(dimethylamine) oxetan-3-yl)methanol (67.6 mg, 516 µmol,1 eq) in THF (5 ml). was added NaH (18.5 mg, 774 µmol) at 0°C, the reaction mixture was stirred at 0 °C for 15 min, then Intermediate 2 (100 mg, 258 µmol) was added to the reaction mixture at 25 °C, the resulting solution was stirred for 4 hours at 80°C. Then it was cooled to room temperature. The resulting solution was diluted with 20 mL of water. The resulting solution was extracted with 2x20 mL of ethyl acetate, the organic layers combined, and the resulting mixture was washed with 20 mL of brine. The mixture was dried over anhydrous sodium sulfate and concentrated under vacuum. The product was purified by chromatography with DCM: MeOH to afford the title compound (120 mg, yield:93.7 %) as a yellow solid. LC-MS: (ES, m/z): RT = 1.037 min, LCMS: m/z = 498 [M+1].
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