2,6-Diisopropylphenyl isocyanate → HCID 21957917, compound

HRID 2213629Notes

Reaction equation

HRID 2213629 reaction equation
[CH2:1]([C:3]1[CH:8]=[CH:7][C:6]([NH:9][CH2:10][C:11]2[CH:16]=[CH:15][C:14]([N:17]3[CH2:22][CH2:21][O:20][CH2:19][CH2:18]3)=[CH:13][CH:12]=2)=[CH:5][CH:4]=1)[CH3:2].[CH:23]([C:26]1[CH:31]=[CH:30][CH:29]=[C:28]([CH:32]([CH3:34])[CH3:33])[C:27]=1[N:35]=[C:36]=[O:37])([CH3:25])[CH3:24]>>[CH:23]([C:26]1[CH:31]=[CH:30][CH:29]=[C:28]([CH:32]([CH3:33])[CH3:34])[C:27]=1[NH:35][C:36](=[O:37])[N:9]([C:6]1[CH:7]=[CH:8][C:3]([CH2:1][CH3:2])=[CH:4][CH:5]=1)[CH2:10][C:11]1[CH:16]=[CH:15][C:14]([N:17]2[CH2:18][CH2:19][O:20][CH2:21][CH2:22]2)=[CH:13][CH:12]=1)([CH3:24])[CH3:25]

Participants

3

Reactant 2

HCID 922592,6-Diisopropylphenyl isocyanateHCID 21957968HCID 21957968, compound

Product 1

HCID 21957917HCID 21957917, compound

Procedure

By the reaction and treatment in the same manner as in Example 1 using (4-ethylphenyl)(4-morpholinophenylmethyl)amine (0.63 g) and 2,6-diisopropylphenyl isocyanate (0.46 mL) as starting materials, N′-(2,6-diisopropylphenyl)-N-(4-ethylphenyl)-N-(4-morpholinophenylmethyl)urea (0.45 g) was obtained. melting point: 159–161° C.

Sources & evidence

ORD record
ord-69147868b1db47079fe909422d663833
Source dataset
uspto-grants-2006_09
Patent number
US07105567B2

Reaction notes

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