HCID 15724942, compound → HCID 15724960, compound

HRID 344729Notes

Reaction equation

HRID 344729 reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([N:8]2[CH:12]=[CH:11][N:10]=[C:9]2[SH:13])[CH:3]=1.[CH3:14][C:15]1[CH:20]=[C:19]([CH3:21])[CH:18]=[C:17]([CH3:22])[C:16]=1[S:23]([NH:26][C:27]1[CH:34]=[CH:33][CH:32]=[CH:31][C:28]=1[CH2:29]Cl)(=[O:25])=[O:24]>>[CH3:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([N:8]2[CH:12]=[CH:11][N:10]=[C:9]2[S:13][CH2:29][C:28]2[CH:31]=[CH:32][CH:33]=[CH:34][C:27]=2[NH:26][S:23]([C:16]2[C:15]([CH3:14])=[CH:20][C:19]([CH3:21])=[CH:18][C:17]=2[CH3:22])(=[O:24])=[O:25])[CH:3]=1

Participants

3

Reactant 2

HCID 15724942HCID 15724942, compoundHCID 178428561HCID 178428561, compound

Product 1

HCID 15724960HCID 15724960, compound

Procedure

1.25 g of 1-(4-methyl-2-pyridyl)-2-mercaptoimidazole and o-(2,4,6-trimethylphenyl)sulfonylaminobenzyl chloride are treated in the same manner as described in Example 1-(1) to give 2.19 g of 1-(4-methyl-2-pyridyl)-2-(2-(2,4,6-trimethylphenyl)sulfonylaminobenzylthio)imidazole.

Sources & evidence

ORD record
ord-05c4c0963e644c3e8cbaec026f5e6eaf
Source dataset
uspto-grants-1991_10
Patent number
US05053417

Reaction notes

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