Water → HCID 57847233, compound

HRID 735762Notes

Reaction equation

HRID 735762 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]1

Participants

6

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

  1. temperaturecooling
  2. extractionextracted with dichloromethane
  3. dry with materialThe extract was dried over anhydrous MgSO4
  4. customthe solvent was evaporated under reduced pressure
  5. 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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