Sulfanilamide → HCID 178424076, compound
Reaction equation
CN1CCN([C:8]2[CH:13]=[CH:12][C:11]([NH:14][C:15]3[N:20]=[C:19]([C:21]4[C:22]([C:26]5[CH:31]=[CH:30][C:29]([CH3:32])=[CH:28][CH:27]=5)=[N:23][NH:24][CH:25]=4)[CH:18]=[CH:17][N:16]=3)=[CH:10][CH:9]=2)CC1.NC1C=CC([S:40]([NH2:43])(=[O:42])=[O:41])=CC=1>>[C:29]1([CH3:32])[CH:30]=[CH:31][C:26]([C:22]2[C:21]([C:19]3[CH:18]=[CH:17][N:16]=[C:15]([NH:14][C:11]4[CH:12]=[CH:13][C:8]([S:40]([NH2:43])(=[O:42])=[O:41])=[CH:9][CH:10]=4)[N:20]=3)=[CH:25][NH:24][N:23]=2)=[CH:27][CH:28]=1Participants
3
Procedure
The title compound is prepared as described in Example 1 using ethyl-4-methylbenzoate (see Example 25) and 4-amino-benzenesulfonamide.
Sources & evidence
- ORD record
- ord-417e1e748f134c12a39a0a444ae1fc96
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07691855B2
Reaction notes
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