Hydrochloric Acid → HCID 69890111, compound
Reaction equation
[C:1]([C:4]1[C:12]2[C:7](=[CH:8][CH:9]=[C:10]([Cl:13])[CH:11]=2)[N:6]([S:14]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)(=[O:16])=[O:15])[CH:5]=1)(=[O:3])[CH3:2].C[O:24][C:25]([C:27]1[CH:28]=[C:29]([CH:33]=[CH:34][CH:35]=1)[C:30](Cl)=[O:31])=[O:26].Cl>>[C:17]1([S:14]([N:6]2[C:7]3[C:12](=[CH:11][C:10]([Cl:13])=[CH:9][CH:8]=3)[C:4]([C:1](=[O:3])[CH:2]=[C:30]([C:29]3[CH:33]=[CH:34][CH:35]=[C:27]([C:25]([OH:26])=[O:24])[CH:28]=3)[OH:31])=[CH:5]2)(=[O:16])=[O:15])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1Participants
4
Procedure
In accordance with Example 99, 3-acetyl-1-benzenesulfonyl-5-chloroindole reacted with 3-methoxycarbonyl benzoylchloride, followed by hydrolysis with hydrochloric acid to give the titled compound.
Sources & evidence
- ORD record
- ord-df9948ddf2b64f8db05e7f52e156d858
- Source dataset
- uspto-grants-2003_01
- Patent number
- US06506787B2
Reaction notes
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