2,4,5-Trichlorobenzenesulfonyl chloride → 2-[2-(2,4,5-Trichlorobenzenesulphonylamino)-ethyl]-1-methylpyrrol
Reaction equation
[NH2:1][CH2:2][CH2:3][C:4]1[N:5]([CH3:9])[CH:6]=[CH:7][CH:8]=1.[Cl:10][C:11]1[CH:16]=[C:15]([Cl:17])[C:14]([Cl:18])=[CH:13][C:12]=1[S:19](Cl)(=[O:21])=[O:20]>>[Cl:10][C:11]1[CH:16]=[C:15]([Cl:17])[C:14]([Cl:18])=[CH:13][C:12]=1[S:19]([NH:1][CH2:2][CH2:3][C:4]1[N:5]([CH3:9])[CH:6]=[CH:7][CH:8]=1)(=[O:21])=[O:20]Participants
3
Procedure
Prepared from 2-(2-aminoethyl)-1-methylpyrrol and 2,4,5-trichlorobenzenesulphonylchloride analogously to Example A.
Sources & evidence
- ORD record
- ord-852195932d6748cd8739d99bc5ac734c
- Source dataset
- uspto-grants-1989_09
- Patent number
- US04870076
Reaction notes
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