Hydrochloric Acid → HCID 118037691, compound
Reaction equation
[CH:1]1([C:4]2[CH:9]=[C:8]([CH2:10][N:11]3[CH2:16][CH2:15][CH:14]([N:17]4[CH:22]=[CH:21][C:20]([C:23]([O:25]C)=[O:24])=[CH:19][C:18]4=[O:27])[CH2:13][CH2:12]3)[C:7]([O:28][CH:29]([CH3:31])[CH3:30])=[CH:6][C:5]=2[C:32]2[CH:37]=[CH:36][C:35]([F:38])=[CH:34][CH:33]=2)[CH2:3][CH2:2]1.[OH-].[Na+].Cl>C(O)C>[CH:1]1([C:4]2[CH:9]=[C:8]([CH2:10][N:11]3[CH2:16][CH2:15][CH:14]([N:17]4[CH:22]=[CH:21][C:20]([C:23]([OH:25])=[O:24])=[CH:19][C:18]4=[O:27])[CH2:13][CH2:12]3)[C:7]([O:28][CH:29]([CH3:31])[CH3:30])=[CH:6][C:5]=2[C:32]2[CH:37]=[CH:36][C:35]([F:38])=[CH:34][CH:33]=2)[CH2:2][CH2:3]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixed solution of methyl 1-(1-((2-cyclopropyl-4′-fluoro-5-isopropoxybiphenyl-4-yl)methyl)piperidin-4-yl)-2-oxo-1,2-dihydropyridine-4-carboxylate (103 mg), a 1 M aqueous sodium hydroxide solution (1 mL), and ethanol (2 mL) was stirred at 70 C for 1 hour. The obtained reaction solution was neutralized with 1 M hydrochloric acid and, in this state, stirred at room temperature for 3 hours. The resulting solid was collected by filtration and recrystallized (ethyl acetate) to obtain the title compound (70.3 mg).
Workup
- customThe obtained reaction solution
- filtrationThe resulting solid was collected by filtration
- customrecrystallized (ethyl acetate)
Sources & evidence
- ORD record
- ord-eb1da2406afd4c8a968a6cc46deabc22
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09120777B2
Reaction notes
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