2,6-Diisopropylphenyl isocyanate → HCID 21957960, compound

HRID 2213619Notes

Reaction equation

HRID 2213619 reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH2:9][NH:10][C:11]2[CH:16]=[CH:15][C:14]([CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])=[CH:13][CH:12]=2)=[CH:5][CH:4]=1)#[N:2].[CH:25]([C:28]1[CH:33]=[CH:32][CH:31]=[C:30]([CH:34]([CH3:36])[CH3:35])[C:29]=1[N:37]=[C:38]=[O:39])([CH3:27])[CH3:26]>>[C:1]([C:3]1[CH:4]=[CH:5][C:6]([CH2:9][N:10]([C:11]2[CH:16]=[CH:15][C:14]([CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])=[CH:13][CH:12]=2)[C:38]([NH:37][C:29]2[C:28]([CH:25]([CH3:26])[CH3:27])=[CH:33][CH:32]=[CH:31][C:30]=2[CH:34]([CH3:36])[CH3:35])=[O:39])=[CH:7][CH:8]=1)#[N:2]

Participants

3

Procedure

By the reaction and treatment in the same manner as in Example 2 using (4-cyanophenylmethyl)(4-octylphenyl)amine (3.65 g) and 2,6-diisopropylphenyl isocyanate (2.55 g) as starting materials, N-(4-cyanophenylmethyl)-N′-(2,6-diisopropylphenyl)-N-(4-octylphenyl)urea (0.49 g) was obtained.

Sources & evidence

ORD record
ord-d163ec1cb1b74a398ff9c23eb8229cb1
Source dataset
uspto-grants-2006_09
Patent number
US07105567B2

Reaction notes

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