Water → HCID 57847233, compound
Reaction equation
Cl.[CH3:2][C:3]1[O:4][CH:5]=[CH:6][C:7]=1[C@H:8]1[C@H:17]2[CH2:18][CH2:19][N:20]([C:21]([C@H:23]3[CH2:28][CH2:27][CH2:26][CH2:25][C@H:24]3[NH2:29])=[O:22])[C@H:16]2[C:15]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[NH:9]1.C(N(CC)CC)C.[C:37](Cl)(=[O:44])[C:38]1[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1.O>ClCCl>[CH3:2][C:3]1[O:4][CH:5]=[CH:6][C:7]=1[C@H:8]1[C@H:17]2[CH2:18][CH2:19][N:20]([C:21]([C@H:23]3[CH2:28][CH2:27][CH2:26][CH2:25][C@H:24]3[NH:29][C:37](=[O:44])[C:38]3[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=3)=[O:22])[C@H:16]2[C:15]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[NH:9]1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of (1R,2S)-2-{[(3aR,4R,9bR)-4-(2-methyl-3-furyl)-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinolin-1-yl]carbonyl}cyclohexaneamine hydrochloride (201 mg, 0.445 mmol) in dichloromethane (5 ml) were added triethylamine (0.203 ml, 1.47 mmol) and benzoylchloride (0.0568 ml, 0.490 mmol) under ice-cooling. The reaction mixture was stirred overnight at room temperature, water was added, and extracted with dichloromethane. The extract was dried over anhydrous MgSO4, and the solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography and eluted with hexane-ethyl acetate (4:1-3:2, v/v) to give the title compound (176 mg, 82%) as an amorphous form.
Workup
- temperaturecooling
- extractionextracted with dichloromethane
- dry with materialThe extract was dried over anhydrous MgSO4
- customthe solvent was evaporated under reduced pressure
- washeluted with hexane-ethyl acetate (4:1-3:2
Sources & evidence
- ORD record
- ord-8c55d398201c48eb822f364a40a332af
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07592453B2
Reaction notes
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