2-Cyclopentyl-2-phenylethanamine → 2-(2,6-Diisopropylphenylsulfamoyl)-N-(2-cyclopentyl-2-phenylethyl)-acetamide

HRID 2396100Notes

Reaction equation

HRID 2396100 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]([NH:20][C:21]1N=NN(CCCCCCCCCCCC)N=1)=[O:19])(=[O:16])=[O:15])([CH3:3])[CH3:2].[CH:38]1([CH:43]([C:46]2[CH:51]=[CH:50][CH:49]=[CH:48][CH:47]=2)CN)[CH2:42][CH2:41][CH2:40][CH2:39]1>>[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]([NH:20][CH2:21][CH:43]([CH:38]1[CH2:39][CH2:40][CH2:41][CH2:42]1)[C:46]1[CH:47]=[CH:48][CH:49]=[CH:50][CH:51]=1)=[O:19])(=[O:15])=[O:16])([CH3:2])[CH3:3]

Participants

3

Reactant 2

HCID 172339682-Cyclopentyl-2-phenylethanamineHCID 189886562-(2,6-Diisopropyl-phenylsulfamoyl)-N-(dodecyl-2-H-tetrazol-5-yl)-acetamide

Product 1

HCID 189886682-(2,6-Diisopropylphenylsulfamoyl)-N-(2-cyclopentyl-2-phenylethyl)-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 2-cyclopentyl-2-phenylethylamine, mp 168°-170° C.

Sources & evidence

ORD record
ord-cb2e8891581341ef96b8041d467df092
Source dataset
uspto-grants-1996_02
Patent number
US05491170

Reaction notes

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