Benzhydrylamine → 2-(2,6-Diisopropylphenylsulfamoyl)-N-diphenylmethylacetamide

HRID 2396099Notes

Reaction equation

[CH:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH:10]([CH3:12])[CH3:11])[C:5]=1[NH:13][S:14]([CH2:17][C:18](NC1N=NN(CCCCCCCCCCCC)N=1)=[O:19])(=[O:16])=[O:15])([CH3:3])[CH3:2].[C:38]1([CH:44]([NH2:51])[C:45]2[CH:50]=[CH:49][CH:48]=[CH:47][CH:46]=2)[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1>>[CH:10]([C:6]1[CH:7]=[CH:8][CH:9]=[C:4]([CH:1]([CH3:3])[CH3:2])[C:5]=1[NH:13][S:14]([CH2:17][C:18]([NH:51][CH:44]([C:45]1[CH:46]=[CH:47][CH:48]=[CH:49][CH:50]=1)[C:38]1[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1)=[O:19])(=[O:16])=[O:15])([CH3:11])[CH3:12]

Participants

Reactant 2

HCID 7036Benzhydrylamine

HCID 189886562-(2,6-Diisopropyl-phenylsulfamoyl)-N-(dodecyl-2-H-tetrazol-5-yl)-acetamide

Product 1

HCID 189886782-(2,6-Diisopropylphenylsulfamoyl)-N-diphenylmethylacetamide

Procedure

This compound was prepared in the same manner as for the title compound of Example 2, except that 2-DAT was replaced with diphenylmethylamine, mp 166°-167° C.

Sources & evidence

ORD record: ord-9c636a08684448a8a5f2cd3c553edcef
Source dataset: uspto-grants-1996_02
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05491170

Reaction notes

Loading…