2,6-Diisopropylphenyl isocyanate → HCID 21957928, compound
Reaction equation
[CH2:1]([NH:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][CH3:16])=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:17]([C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([CH:26]([CH3:28])[CH3:27])[C:21]=1[N:29]=[C:30]=[O:31])([CH3:19])[CH3:18]>>[CH2:1]([N:8]([C:9]1[CH:10]=[CH:11][C:12]([CH2:15][CH3:16])=[CH:13][CH:14]=1)[C:30]([NH:29][C:21]1[C:20]([CH:17]([CH3:18])[CH3:19])=[CH:25][CH:24]=[CH:23][C:22]=1[CH:26]([CH3:28])[CH3:27])=[O:31])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
By the reaction and treatment in the same manner as in Example 2 using benzyl(4-ethylphenyl)amine (1.77 g) and 2,6-diisopropylphenyl isocyanate (1.96 g) as starting materials, N-benzyl-N′-(2,6-diisopropylphenyl)-N-(4-ethylphenyl)urea (1.49 g) was obtained.
Sources & evidence
- ORD record
- ord-387302c4201e475098b40c8f5ece24bd
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07105567B2
Reaction notes
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