2,6-Diisopropylphenyl isocyanate → HCID 10117638, compound

HRID 2213642Notes

Reaction equation

HRID 2213642 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:9][NH:10][C:11]2[CH:16]=[CH:15][C:14]([CH:17]([CH3:19])[CH3:18])=[CH:13][CH:12]=2)[CH:5]=[CH:6][C:7]=1[Cl:8].[CH:20]([C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([CH:29]([CH3:31])[CH3:30])[C:24]=1[N:32]=[C:33]=[O:34])([CH3:22])[CH3:21]>>[Cl:1][C:2]1[CH:3]=[C:4]([CH2:9][N:10]([C:11]2[CH:16]=[CH:15][C:14]([CH:17]([CH3:19])[CH3:18])=[CH:13][CH:12]=2)[C:33]([NH:32][C:24]2[C:23]([CH:20]([CH3:21])[CH3:22])=[CH:28][CH:27]=[CH:26][C:25]=2[CH:29]([CH3:31])[CH3:30])=[O:34])[CH:5]=[CH:6][C:7]=1[Cl:8]

Participants

3

Reactant 2

HCID 922592,6-Diisopropylphenyl isocyanateHCID 21957970HCID 21957970, compound

Product 1

HCID 10117638HCID 10117638, compoundYield 28.4%

Procedure

By the reaction and treatment in the same manner as in Example 2 using [(3,4-dichlorophenyl)methyl](4-isopropylphenyl)amine (2.5 g) and 2,6-diisopropylphenyl isocyanate (2.7 g) as starting materials, N-(3,4-dichlorophenylmethyl)-N′-(2,6-diisopropylphenyl)-N-(4-isopropylphenyl)urea (1.2 g) was obtained.

Sources & evidence

ORD record
ord-4d98a8a9efd946e1b39cd0f3b70b5792
Source dataset
uspto-grants-2006_09
Patent number
US07105567B2

Reaction notes

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