2'-Nitro-4-biphenylyl-sulphonic acid chloride → HCID 178428643, compound

HRID 274975Notes

Reaction equation

HRID 274975 reaction equation
[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][CH:11]([NH2:21])[C:12]([N:14]3[CH2:19][CH2:18][CH:17]([CH3:20])[CH2:16][CH2:15]3)=[O:13])=[CH:9][C:4]=2[N:3]=[CH:2]1.[N+:22]([C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=1[C:31]1[CH:36]=[CH:35][C:34]([S:37](Cl)(=[O:39])=[O:38])=[CH:33][CH:32]=1)([O-:24])=[O:23]>>[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][CH:11]([NH:21][S:37]([C:34]3[CH:33]=[CH:32][C:31]([C:26]4[CH:27]=[CH:28][CH:29]=[CH:30][C:25]=4[N+:22]([O-:24])=[O:23])=[CH:36][CH:35]=3)(=[O:38])=[O:39])[C:12]([N:14]3[CH2:19][CH2:18][CH:17]([CH3:20])[CH2:16][CH2:15]3)=[O:13])=[CH:9][C:4]=2[N:3]=[CH:2]1

Participants

3

Reactant 2

HCID 218061172'-Nitro-4-biphenylyl-sulphonic acid chlorideHCID 178428665HCID 178428665, compound

Product 1

HCID 178428643HCID 178428643, compound

Procedure

Prepared from 1-(1H-benzimidazol-5-yl-methyl)-2-(4-methyl-piperidin-1-yl)-2-oxo-ethylamine and 2'-nitro-4-biphenylyl-sulphonic acid chloride analogously to Example 2.

Sources & evidence

ORD record
ord-b9775ba961bb4e4da4112db7f80b3b39
Source dataset
uspto-grants-1995_02
Patent number
US05391556

Reaction notes

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