1-Hexanol → HCID 44331258, compound

HRID 2396112Notes

Reaction equation

HRID 2396112 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].[CH2:38]([OH:44])[CH2:39][CH2:40][CH2:41][CH2:42][CH3:43]>>[CH2:38]([O:44][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])[CH2:39][CH2:40][CH2:41][CH2:42][CH3:43]

Participants

3

Reactant 2

HCID 81031-HexanolHCID 189886562-(2,6-Diisopropyl-phenylsulfamoyl)-N-(dodecyl-2-H-tetrazol-5-yl)-acetamide

Product 1

HCID 44331258HCID 44331258, compound

Procedure

This compound was prepared in the same manner as for the title compound of Example 2, except that 2-DAT was replaced with hexanol, mp 66°-68° C.

Sources & evidence

ORD record
ord-f0101bd2ca954446a40e8de34e1b871c
Source dataset
uspto-grants-1996_02
Patent number
US05491170

Reaction notes

Loading…