Isopropylbenzylamine → N-Benzyl-2-(2,6-diisopropyl-phenylsulfamoyl)-N-isopropyl-acetamide

HRID 2396098Notes

Reaction equation

HRID 2396098 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].[CH:38]([NH:41][CH2:42][C:43]1[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=1)([CH3:40])[CH3:39]>>[CH2:42]([N:41]([CH:38]([CH3:40])[CH3:39])[C:18](=[O:19])[CH2:17][S:14](=[O:15])(=[O:16])[NH:13][C:5]1[C:6]([CH:10]([CH3:12])[CH3:11])=[CH:7][CH:8]=[CH:9][C:4]=1[CH:1]([CH3:2])[CH3:3])[C:43]1[CH:48]=[CH:47][CH:46]=[CH:45][CH:44]=1

Participants

3

Reactant 2

HCID 66024IsopropylbenzylamineHCID 189886562-(2,6-Diisopropyl-phenylsulfamoyl)-N-(dodecyl-2-H-tetrazol-5-yl)-acetamide

Product 1

HCID 15341057N-Benzyl-2-(2,6-diisopropyl-phenylsulfamoyl)-N-isopropyl-acetamide

Procedure

This compound was prepared in the same manner as for the title compound of Example 2, except that 2-DAT was replaced with N-isopropyl-N-benzylamine, mp 168°-170° C.

Sources & evidence

ORD record
ord-7231a6b1c7c8448284b72adc2ed5d4d5
Source dataset
uspto-grants-1996_02
Patent number
US05491170

Reaction notes

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