1-Methyl-4-piperidone → HCID 22611387, compound
Reaction equation
[CH3:1][N:2]([S:4]([NH:7][C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[NH:13][CH:12]=[CH:11]2)(=[O:6])=[O:5])[CH3:3].[CH3:17][N:18]1[CH2:23][CH2:22][C:21](=O)[CH2:20][CH2:19]1>>[CH3:3][N:2]([S:4]([NH:7][C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[NH:13][CH:12]=[C:11]2[C:21]1[CH2:22][CH2:23][N:18]([CH3:17])[CH2:19][CH:20]=1)(=[O:6])=[O:5])[CH3:1]Participants
3
Procedure
Beginning with 1.17 gm (4.89 mMol) 5-(N,N-dimethylamino)sulfonylamino-1H-indole and 0.78 mL (6.4 mMol) 1-methyl-4-piperidone, 1.19 gm (72.6%) of the title compound were recovered as a pale yellow powder.
Sources & evidence
- ORD record
- ord-174aece1e56242f4921203e460f60dee
- Source dataset
- uspto-grants-1999_10
- Patent number
- US05962474
Reaction notes
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