2,6-Diisopropylphenyl isocyanate → HCID 21957967, compound
Reaction equation
[C:1]1([C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH:6]=[CH:5][C:4]([CH2:7][NH:8][C:9]2[CH:14]=[CH:13][C:12]([CH:15]([CH3:17])[CH3:16])=[CH:11][CH:10]=2)=[CH:3][CH:2]=1.[CH:24]([C:27]1[CH:32]=[CH:31][CH:30]=[C:29]([CH:33]([CH3:35])[CH3:34])[C:28]=1[N:36]=[C:37]=[O:38])([CH3:26])[CH3:25]>>[C:1]1([C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=2)[CH:2]=[CH:3][C:4]([CH2:7][N:8]([C:9]2[CH:14]=[CH:13][C:12]([CH:15]([CH3:17])[CH3:16])=[CH:11][CH:10]=2)[C:37]([NH:36][C:28]2[C:27]([CH:24]([CH3:25])[CH3:26])=[CH:32][CH:31]=[CH:30][C:29]=2[CH:33]([CH3:35])[CH3:34])=[O:38])=[CH:5][CH:6]=1Participants
3
Procedure
By the reaction and treatment in the same manner as in Example 2 using (4-biphenylylmethyl)(4-isopropylphenyl)amine (1.0 g) and 2,6-diisopropylphenyl isocyanate (0.88 g) as starting materials, N-(4-biphenylylmethyl)-N′-(2,6-diisopropylphenyl)-N-(4-isopropylphenyl)urea (0.88 g) was obtained.
Sources & evidence
- ORD record
- ord-7da99e7df8f04651987ab7d04c6d78b2
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07105567B2
Reaction notes
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