4-Nitrobenzenesulfonyl chloride → 2-[2-(p-Nitrobenzenesulphonylamino)-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.[N+:10]([C:13]1[CH:18]=[CH:17][C:16]([S:19](Cl)(=[O:21])=[O:20])=[CH:15][CH:14]=1)([O-:12])=[O:11]>>[N+:10]([C:13]1[CH:14]=[CH:15][C:16]([S:19]([NH:1][CH2:2][CH2:3][C:4]2[N:5]([CH3:9])[CH:6]=[CH:7][CH:8]=2)(=[O:21])=[O:20])=[CH:17][CH:18]=1)([O-:12])=[O:11]Participants
3
Procedure
Prepared from 2-(2-aminoethyl)-1-methylpyrrol and p-nitrobenzenesulphonylchloride analogously to Example A.
Sources & evidence
- ORD record
- ord-495d46165556420982a844887691d138
- Source dataset
- uspto-grants-1989_09
- Patent number
- US04870076
Reaction notes
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