Piperidine → 2-(piperidin-1-ylsulfonyl)aniline
Reaction equation
[NH:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[N+:7]([C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[S:16](Cl)(=[O:18])=[O:17])([O-])=O>>[N:1]1([S:16]([C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=2[NH2:7])(=[O:18])=[O:17])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
3
Procedure
The title compound (0.59 g, 58%) was obtained as a brown solid from piperidine and 2-nitrobenzenesulfonylchloride following the same procedure as described in preparation 2.
Sources & evidence
- ORD record
- ord-3189dae6040541e9915a6a38aea97f8b
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07253171B2
Reaction notes
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