Benzoyl chloride → HCID 12608535, compound
Reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([C:10](=[O:24])[CH2:11][CH2:12][CH2:13][N:14]2[CH2:19][CH2:18][CH:17]([NH:20][C:21]([NH2:23])=[O:22])[CH2:16][CH2:15]2)=[CH:2]1.[C:25](Cl)(=[O:32])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>>[C:25]([NH:23][C:21]([NH:20][CH:17]1[CH2:16][CH2:15][N:14]([CH2:13][CH2:12][CH2:11][C:10]([C:3]2[C:4]3[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=3)[NH:1][CH:2]=2)=[O:24])[CH2:19][CH2:18]1)=[O:22])(=[O:32])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1Participants
3
Procedure
The product may be prepared by the alternative method of treating 1-[1-(4-[3-indolyl]-4-oxobutyl)piperid-4-yl]urea with benzoyl chloride following the procedure of Example 1.
Sources & evidence
- ORD record
- ord-5dcfc5b10faf43c9b69012e127dd7a87
- Source dataset
- uspto-grants-1977_12
- Patent number
- US04061641
Reaction notes
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