4-Toluenesulfonyl chloride → 2-[2-(p-Toluenesulphonylamino)-ethyl]-1-methylpyrrole
Reaction equation
[NH2:1][CH2:2][CH2:3][C:4]1[N:5]([CH3:9])[CH:6]=[CH:7][CH:8]=1.[C:10]1([CH3:20])[CH:15]=[CH:14][C:13]([S:16](Cl)(=[O:18])=[O:17])=[CH:12][CH:11]=1>>[C:10]1([CH3:20])[CH:15]=[CH:14][C:13]([S:16]([NH:1][CH2:2][CH2:3][C:4]2[N:5]([CH3:9])[CH:6]=[CH:7][CH:8]=2)(=[O:18])=[O:17])=[CH:12][CH:11]=1Participants
3
Procedure
Prepared from 2-(2-aminoethyl)-1-methylpyrrol and p-toluenesulphonylchloride analogously to Example A.
Sources & evidence
- ORD record
- ord-96ccbd7511234dbb93e66931992f1361
- Source dataset
- uspto-grants-1989_09
- Patent number
- US04870076
Reaction notes
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