Water → HCID 58246280, compound
Reaction equation
C(OC([N:6]1[CH2:11][CH2:10][N:9]([S:12](=[O:39])(=[O:38])[NH:13][CH2:14][CH2:15][O:16][C:17]2[CH:26]=[C:25]3[C:20]([CH2:21][CH2:22][N:23]=[C:24]3[C:27]3([C:31]4[CH:36]=[CH:35][C:34]([Cl:37])=[CH:33][CH:32]=4)[CH2:30][CH2:29][CH2:28]3)=[CH:19][CH:18]=2)[CH2:8][CH2:7]1)=O)C.[OH-].[K+].O>C(O)C>[Cl:37][C:34]1[CH:33]=[CH:32][C:31]([C:27]2([C:24]3[C:25]4[C:20](=[CH:19][CH:18]=[C:17]([O:16][CH2:15][CH2:14][NH:13][S:12]([N:9]5[CH2:10][CH2:11][NH:6][CH2:7][CH2:8]5)(=[O:38])=[O:39])[CH:26]=4)[CH2:21][CH2:22][N:23]=3)[CH2:30][CH2:29][CH2:28]2)=[CH:36][CH:35]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
4-(2-{1-[1-(4-Chloro-phenyl)-cyclobutyl]-3,4-dihydro-isoquinolin-7-yloxy}-ethylsulfamoyl)-piperazine-1-carboxylic acid ethyl ester (450 mg, 0.782 mmol, example 54, procedure 1) and a 10% solution of potassium hydroxid in ethanol (20 ml) were heated under reflux for 15 h. The solvent was reduced and water was added to the residue. The mixture was extracted with dichloromethane. The combined organic layers were washed with sodium chloride, dried with potassium sulphate and evaporated. The residue was purified by column chromatography with silica gel using dichloromethane/methanol 3%->5% as the eluent to give the desired product as a yellow oil (394 mg, 0.782 mmol, 61%).
Workup
- temperatureunder reflux for 15 h
- extractionThe mixture was extracted with dichloromethane
- washThe combined organic layers were washed with sodium chloride
- dry with materialdried with potassium sulphate
- customevaporated
- customThe residue was purified by column chromatography with silica gel
Sources & evidence
- ORD record
- ord-725022895cce4397899f52bb23b0863e
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08653100B2
Reaction notes
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