2,6-Diisopropylphenyl isocyanate → HCID 21957914, compound

HRID 2213649Notes

Reaction equation

HRID 2213649 reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][NH:9][C:10]2[CH:15]=[CH:14][C:13]([CH:16]([CH3:18])[CH3:17])=[CH:12][CH:11]=2)=[CH:4][C:3]=1[O:19][CH3:20].[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:9]([CH2:8][C:5]1[CH:6]=[CH:7][C:2]([OH:1])=[C:3]([O:19][CH3:20])[CH:4]=1)[C:10]1[CH:15]=[CH:14][C:13]([CH:16]([CH3:18])[CH3:17])=[CH:12][CH:11]=1)([CH3:22])[CH3:23]

Participants

3

Procedure

By the reaction and treatment in the same manner as in Example 2 using (4-hydroxy-3-methoxyphenylmethyl)(4-isopropylphenyl)amine (7.0 g) and 2,6-diisopropylphenyl isocyanate (5.5 mL) as starting materials, N′-(2,6-diisopropylphenyl)-N-[(4-hydroxy-3-methoxyphenyl)methyl]-N-(4-isopropylphenyl)urea (0.65 g) was obtained.

Sources & evidence

ORD record
ord-c4f32dd1a6bd4075804d3aa9543c352f
Source dataset
uspto-grants-2006_09
Patent number
US07105567B2

Reaction notes

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