Hydrochloric Acid → HCID 86700081, compound
Reaction equation
C(O)C.[ClH:4].[NH2:5][C:6]1[C:11]([C:12]2[CH:17]=[CH:16][C:15]([NH:18][C:19]([C:21]3[C:26](=[O:27])[C:25]([C:28]4[CH:33]=[CH:32][C:31]([F:34])=[CH:30][CH:29]=4)=[CH:24][N:23]([CH2:35][C:36]([F:39])([F:38])[F:37])[CH:22]=3)=[O:20])=[CH:14][CH:13]=2)=[CH:10][C:9]([C:40]2[CH:45]=[CH:44][C:43]([O:46][CH3:47])=[C:42]([O:48][CH3:49])[CH:41]=2)=[CH:8][N:7]=1>O>[ClH:4].[NH2:5][C:6]1[C:11]([C:12]2[CH:13]=[CH:14][C:15]([NH:18][C:19]([C:21]3[C:26](=[O:27])[C:25]([C:28]4[CH:29]=[CH:30][C:31]([F:34])=[CH:32][CH:33]=4)=[CH:24][N:23]([CH2:35][C:36]([F:37])([F:38])[F:39])[CH:22]=3)=[O:20])=[CH:16][CH:17]=2)=[CH:10][C:9]([C:40]2[CH:45]=[CH:44][C:43]([O:46][CH3:47])=[C:42]([O:48][CH3:49])[CH:41]=2)=[CH:8][N:7]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 40 °C
Procedure
Ethanol (14.8 ml), concentrated hydrochloric acid (as 12 mol/L) (219 μl, 1.05 eq.) and water (6 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 (1.50 g, 2.43 mmol) at room temperature. The mixture was stirred at 40° C. for about 11 hours and then at room temperature for one hour, and the precipitated solid was collected by filtration. The solid was then dried under reduced pressure at room temperature for three hours to give the title compound (1.54 g). Yield: 97%.
Workup
- waitat room temperature for one hour
- filtrationthe precipitated solid was collected by filtration
- customThe solid was then dried under reduced pressure at room temperature for three hours
Sources & evidence
- ORD record
- ord-8a396aac49bb447380c1c4a86f525505
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08933103B2
Reaction notes
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