2,6-Diisopropylphenyl isocyanate → HCID 10205719, compound

HRID 2213655Notes

Reaction equation

HRID 2213655 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]([S:18][CH3:19])=[CH:14][CH:13]=2)=[CH:6][CH:5]=1)([CH3:3])[CH3:2].[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]>>[CH:20]([C:23]1[CH:28]=[CH:27][CH:26]=[C:25]([CH:29]([CH3:30])[CH3:31])[C:24]=1[NH:32][C:33](=[O:34])[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]([S:18][CH3:19])=[CH:16][CH:17]=1)([CH3:21])[CH3:22]

Participants

3

Reactant 2

HCID 922592,6-Diisopropylphenyl isocyanateHCID 28512415HCID 28512415, compound

Product 1

HCID 10205719HCID 10205719, compoundYield 82.9%

Procedure

By the reaction and treatment in the same manner as in Example 2 using (4-isopropylphenyl)[(4-methylthiophenyl)methyl]amine (2.0 g) and 2,6-diisopropylphenyl isocyanate (2.1 g) as starting materials, N′-(2,6-diisopropylphenyl)-N-(4-isopropylphenyl)-N-[(4-methylthiophenyl)methyl]urea (2.9 g) was obtained.

Sources & evidence

ORD record
ord-b7f6c6665d9d4bd7aa43b96e7ec19915
Source dataset
uspto-grants-2006_09
Patent number
US07105567B2

Reaction notes

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