Hydrochloric Acid → HCID 86700081, compound
Reaction equation
C(O)CC.[ClH:5].[NH2:6][C:7]1[C:12]([C:13]2[CH:18]=[CH:17][C:16]([NH:19][C:20]([C:22]3[C:27](=[O:28])[C:26]([C:29]4[CH:34]=[CH:33][C:32]([F:35])=[CH:31][CH:30]=4)=[CH:25][N:24]([CH2:36][C:37]([F:40])([F:39])[F:38])[CH:23]=3)=[O:21])=[CH:15][CH:14]=2)=[CH:11][C:10]([C:41]2[CH:46]=[CH:45][C:44]([O:47][CH3:48])=[C:43]([O:49][CH3:50])[CH:42]=2)=[CH:9][N:8]=1>O>[ClH:5].[NH2:6][C:7]1[C:12]([C:13]2[CH:14]=[CH:15][C:16]([NH:19][C:20]([C:22]3[C:27](=[O:28])[C:26]([C:29]4[CH:30]=[CH:31][C:32]([F:35])=[CH:33][CH:34]=4)=[CH:25][N:24]([CH2:36][C:37]([F:38])([F:39])[F:40])[CH:23]=3)=[O:21])=[CH:17][CH:18]=2)=[CH:11][C:10]([C:41]2[CH:46]=[CH:45][C:44]([O:47][CH3:48])=[C:43]([O:49][CH3:50])[CH:42]=2)=[CH:9][N:8]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 40 °C
Procedure
1-Propanol (401 μl), a 5.877 mmol/L aqueous hydrochloric acid solution (6.22 μl, 1.10 eq.) and water (4.1 μl) were added to N-{4-[2-amino-5-(3,4-dimethoxyphenyl)pyridin-3-yl]phenyl}-5-(4-fluorophenyl)-4-oxo-1-(2,2,2-trifluoroethyl)-1,4-dihydropyridine-3-carboxamide (20.55 mg, 33.22 μmol) at room temperature, and the mixture was stirred at 40° C. for about 24 hours. After leaving to stand at room temperature for about 30 minutes, the precipitated solid was collected by filtration. The solid was then dried at room temperature to give the title compound (19.65 mg). Yield: 90%.
Workup
- customAfter leaving
- waitto stand at room temperature for about 30 minutes
- filtrationthe precipitated solid was collected by filtration
- customThe solid was then dried at room temperature
Sources & evidence
- ORD record
- ord-f735c90d0b434930b8a2cf800c1bd0df
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08933103B2
Reaction notes
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