Dodecylamine → 2-(2,6-Diisopropyl-phenylsulfamoyl)-N-dodecyl-acetamide
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].[CH2:38](N)[CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH2:48]C>>[CH:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH:10]([CH3:11])[CH3:12])[C:5]=1[NH:13][S:14]([CH2:17][C:18]([NH:20][CH2:21][CH2:48][CH2:47][CH2:46][CH2:45][CH2:44][CH2:43][CH2:42][CH2:41][CH2:40][CH2:39][CH3:38])=[O:19])(=[O:15])=[O:16])([CH3:3])[CH3:2]Participants
3
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-dodecylamine, mp 83°-85° C.
Sources & evidence
- ORD record
- ord-34987f93adfe4eccb5efc63331fe19fb
- Source dataset
- uspto-grants-1996_02
- Patent number
- US05491170
Reaction notes
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