1-(3-Nitrophenylsulfonyl)piperidine → 3-(Piperidinosulfonyl)aniline

HRID 1814647

Reaction equation

HRID 1814647 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([S:10]([N:13]2[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]2)(=[O:12])=[O:11])[CH:7]=[CH:8][CH:9]=1)([O-])=O.N(C1C=C(S(N(C)C)(=O)=O)C=CC=1)=C=O>>[N:13]1([S:10]([C:6]2[CH:5]=[C:4]([NH2:1])[CH:9]=[CH:8][CH:7]=2)(=[O:12])=[O:11])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18]1

Participants

3

Procedure

3-(Piperidine-1-sulfonyl)phenylamine was prepared as described above from 1-(3-nitro-benzenesulfonyl)piperidine. 3-Isocyanato-N,N-dimethylbenzenesulfonamide

Sources & evidence

ORD record
ord-15c4aed6be3f439f99634bcf3be33a67
Source dataset
uspto-grants-2005_04
Patent number
US06875760B2

Linked notes

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