Methanesulfonyl chloride → HCID 483555, compound
Reaction equation
[C:1]1([S:7]([C:10]2[C:18]3[C:13](=[CH:14][CH:15]=[C:16]([NH2:19])[CH:17]=3)[NH:12][C:11]=2[C:20]([NH2:22])=[O:21])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:23][S:24](Cl)(=[O:26])=[O:25]>>[C:1]1([S:7]([C:10]2[C:18]3[C:13](=[CH:14][CH:15]=[C:16]([NH:19][S:24]([CH3:23])(=[O:26])=[O:25])[CH:17]=3)[NH:12][C:11]=2[C:20]([NH2:22])=[O:21])(=[O:8])=[O:9])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
3
Procedure
Reaction of 3-phenylsulfonyl-5-aminoindole-2-carboxamide with methanesulfonyl chloride under the conditions of Example 47 provides the title compound.
Sources & evidence
- ORD record
- ord-47786c283df24d208063cffea84bc574
- Source dataset
- uspto-grants-1996_06
- Patent number
- US05527819
Reaction notes
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