HCID 54001924, compound → HCID 14459101, compound

HRID 344722Notes

Reaction equation

HRID 344722 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[N:7]1[CH:11]=[CH:10][N:9]=[C:8]1[SH:12].[CH3:13][C:14]1[CH:19]=[C:18]([CH3:20])[CH:17]=[C:16]([CH3:21])[C:15]=1[S:22]([NH:25][CH:26](Cl)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)(=[O:24])=[O:23]>>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[N:7]1[CH:11]=[CH:10][N:9]=[C:8]1[S:12][CH2:28][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][C:26]=1[NH:25][S:22]([C:15]1[C:16]([CH3:21])=[CH:17][C:18]([CH3:20])=[CH:19][C:14]=1[CH3:13])(=[O:23])=[O:24]

Participants

3

Reactant 2

HCID 54001924HCID 54001924, compoundHCID 178527868HCID 178527868, compound

Product 1

HCID 14459101HCID 14459101, compoundYield 87%

Procedure

1-(2-pyridyl)-2-mercaptoimidazole and (2,4,6-trimethylphenyl)sulfonylaminobenzyl chloride are treated in the same manner as described in Example 1-(1) to give 1-(2-pyridyl)-2-[2-(2,4,6-trimethylphenyl)sulfonylaminobenzylthio]imidazole.

Sources & evidence

ORD record
ord-631e1a7021514c6f9cb985fbe44de881
Source dataset
uspto-grants-1991_10
Patent number
US05053417

Reaction notes

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