Cyclopentylamine → N-cyclopentyl-3-dimethylamino-1,2,3,4-tetrahydro-9H-carbazole-6-carboxamide
Reaction equation
[CH3:1][N:2]([CH3:19])[CH:3]1[CH2:15][C:14]2[C:13]3[C:8](=[CH:9][CH:10]=[C:11]([C:16]([OH:18])=O)[CH:12]=3)[NH:7][C:6]=2[CH2:5][CH2:4]1.[CH:20]1([NH2:25])[CH2:24][CH2:23][CH2:22][CH2:21]1>>[CH:20]1([NH:25][C:16]([C:11]2[CH:12]=[C:13]3[C:8](=[CH:9][CH:10]=2)[NH:7][C:6]2[CH2:5][CH2:4][CH:3]([N:2]([CH3:1])[CH3:19])[CH2:15][C:14]3=2)=[O:18])[CH2:24][CH2:23][CH2:22][CH2:21]1Participants
3
Procedure
Beginning with 7.4 mg (0.029 mMol) 3-dimethylamino-1,2,3,4-tetrahydro-9H-carbazole-6-carboxylic acid and cyclopentylamine, 4.1 mg (41%) of the title compound were recovered.
Sources & evidence
- ORD record
- ord-5726dad07e6a4f599a49a6ed2d851c54
- Source dataset
- uspto-grants-2001_04
- Patent number
- US06221884B1
Reaction notes
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