2,2-Diphenylethylamine → N-(2,2-Diphenylethyl)-N'-[2,6-di(propan-2-yl)phenyl]urea
Reaction equation
[CH3:1][CH:2]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH:10]([CH3:12])[CH3:11])[C:5]=1[N:13]=[C:14]=[O:15])[CH3:3].[C:16]1([CH:22]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)[CH2:23][NH2:24])[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>>[CH3:3][CH:2]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH:10]([CH3:11])[CH3:12])[C:5]=1[NH:13][C:14]([NH:24][CH2:23][CH:22]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)=[O:15])[CH3:1]Participants
3
Procedure
The title compound, mp 175°-176° C., was prepared from 2,6-bis(1-methylethyl)phenyl isocyanate and 2,2-diphenylethylamine according to the method of Example 1.
Sources & evidence
- ORD record
- ord-0189f10cdd0244b79d58f51c625acbe6
- Source dataset
- uspto-grants-1992_05
- Patent number
- US05116848
Reaction notes
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