2,6-Diisopropylphenyl isocyanate → HCID 10140102, compound
Reaction equation
[CH:1]([C:4]1[CH:9]=[CH:8][C:7]([NH:10][CH2:11][C:12]2[CH:17]=[CH:16][C:15]([CH:18]([CH3:20])[CH3:19])=[CH:14][CH:13]=2)=[CH:6][CH:5]=1)([CH3:3])[CH3:2].[CH:21]([C:24]1[CH:29]=[CH:28][CH:27]=[C:26]([CH:30]([CH3:32])[CH3:31])[C:25]=1[N:33]=[C:34]=[O:35])([CH3:23])[CH3:22]>>[CH:21]([C:24]1[CH:29]=[CH:28][CH:27]=[C:26]([CH:30]([CH3:31])[CH3:32])[C:25]=1[NH:33][C:34](=[O:35])[N:10]([C:7]1[CH:8]=[CH:9][C:4]([CH:1]([CH3:3])[CH3:2])=[CH:5][CH:6]=1)[CH2:11][C:12]1[CH:13]=[CH:14][C:15]([CH:18]([CH3:20])[CH3:19])=[CH:16][CH:17]=1)([CH3:22])[CH3:23]Participants
3
Procedure
By the reaction and treatment in the same manner as in Example 2 using (4-isopropylphenyl)[(4-isopropylphenyl)methyl]amine (1.0 g) and 2,6-diisopropylphenyl isocyanate (0.99 g) as starting materials, N′-(2,6-diisopropylphenyl)-N-(4-isopropylphenyl)-N-[(4-isopropylphenyl)methyl]urea (0.37 g) was obtained.
Sources & evidence
- ORD record
- ord-944325137b2c4277ab02b3dc09ad3338
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07105567B2
Reaction notes
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