Toluene → HCID 19030882, compound
Reaction equation
FC(F)(F)C(O)=O.[OH:8][CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:37]=[CH:36][C:16]([C:17]([N:19]2[CH2:24][CH2:23][CH:22]([N:25]3[C:35]4[C:30](=[CH:31][CH:32]=[CH:33][CH:34]=4)[CH2:29][CH2:28][C:26]3=[O:27])[CH2:21][CH2:20]2)=[O:18])=[CH:15][CH:14]=1.[O:38]([C:40]#[N:41])[Na].C1(C)C=CC=CC=1>C(OCC)(=O)C.C(Cl)(Cl)Cl>[C:40]([O:8][CH2:9][CH2:10][CH2:11][O:12][C:13]1[CH:14]=[CH:15][C:16]([C:17]([N:19]2[CH2:20][CH2:21][CH:22]([N:25]3[C:35]4[C:30](=[CH:31][CH:32]=[CH:33][CH:34]=4)[CH2:29][CH2:28][C:26]3=[O:27])[CH2:23][CH2:24]2)=[O:18])=[CH:36][CH:37]=1)(=[O:38])[NH2:41]Participants
Procedure
Trifluoroacetic acid (0.21 ml) is added dropwise with stirring to a mixture of 1-{1-[4-(3-hydroxypropoxy)benzoyl]-4-piperidinyl}-3,4-dihydrocarbostyril (0.51 g), NaOCN (0.16 g), toluene (5 ml) and chloroform (5 ml) at room temperature. After adding, the mixture is stirred at room temperature overnight. Ethyl acetate is added to the reaction mixture and the mixture is washed with saturated aqueous sodium hydrogen carbonate solution, water and saline solution successively and then dried with sodium sulfate. The solvent is distilled off and the resulting residue is purified by silica gel column chromatography (solvent; dichloromethane:methanol=100:1) to give 1-{1-[4-(3-carbamoyloxypropoxy)benzoyl-4-piperidinyl}-3,4-dihydrocarbostyril (0.15 g).
Workup
- additionAfter adding
- washthe mixture is washed with saturated aqueous sodium hydrogen carbonate solution, water and saline solution successively
- dry with materialdried with sodium sulfate
- distillationThe solvent is distilled off
- customthe resulting residue is purified by silica gel column chromatography (solvent; dichloromethane:methanol=100:1)
Sources & evidence
- ORD record
- ord-045eeadba2a24ab28847b3d7a8bb2502
- Source dataset
- uspto-grants-1997_07
- Patent number
- US05652247
Reaction notes
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