Potassium Carbonate → HCID 86592041, compound
Reaction equation
C[O:2][C:3](=[O:38])[CH:4]=[CH:5][C:6]1[CH:7]=[C:8]2[C:13](=[CH:14][CH:15]=1)[N:12]([C:16](=[O:24])[C:17]1[CH:22]=[CH:21][C:20]([F:23])=[CH:19][CH:18]=1)[C@@H:11]([CH3:25])[CH2:10][C@H:9]2[N:26]([C:31]1[CH:36]=[CH:35][C:34]([Cl:37])=[CH:33][CH:32]=1)[C:27](=[O:30])[CH2:28][CH3:29].C([O-])([O-])=O.[K+].[K+]>CO.O>[Cl:37][C:34]1[CH:35]=[CH:36][C:31]([N:26]([C:27](=[O:30])[CH2:28][CH3:29])[C@H:9]2[C:8]3[C:13](=[CH:14][CH:15]=[C:6]([CH:5]=[CH:4][C:3]([OH:38])=[O:2])[CH:7]=3)[N:12]([C:16](=[O:24])[C:17]3[CH:18]=[CH:19][C:20]([F:23])=[CH:21][CH:22]=3)[C@@H:11]([CH3:25])[CH2:10]2)=[CH:32][CH:33]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of (±)-cis-3-[4-[(4-chloro-phenyl)-propionyl-amino]-1-(4-fluoro-benzoyl)-2-methyl-1,2,3,4-tetrahydro-quinolin-6-yl]-acrylic acid methyl ester (110 mg, 0.21 mmol) in 4 ml methanol was added 50 mg K2CO3, (0.36 mmol, in 2 ml water). The resulting reaction mixture was stirred at room temperature overnight. The methanol was removed under vacuum. 1M HCl was added until the mixture was acidic. Dichloromethane (25 ml) was added. Organic layer was dried with magnesium sulfate. Dichloromethane was removed under vacuum. The residue was purified by HPLC to give 10 mg title compound
Workup
- customThe resulting reaction mixture
- customThe methanol was removed under vacuum
- addition1M HCl was added until the mixture
- additionDichloromethane (25 ml) was added
- dry with materialOrganic layer was dried with magnesium sulfate
- customDichloromethane was removed under vacuum
- customThe residue was purified by HPLC
Sources & evidence
- ORD record
- ord-46a50bcc09fe4487b36933e79bf6e115
- Source dataset
- uspto-grants-2007_05
- Patent number
- US07211672B2
Reaction notes
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