Phenyl isocyanate → HCID 10095117, compound

HRID 1837589Notes

Reaction equation

HRID 1837589 reaction equation
[NH2:1][CH2:2][C:3]([CH3:24])([CH3:23])[CH2:4][N:5]1[C:17]2[C:16]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[N:10]=[C:9]([NH2:18])[C:8]=2[N:7]=[C:6]1[CH2:19][CH2:20][O:21][CH3:22].[C:25]1([N:31]=[C:32]=[O:33])[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1>>[NH2:18][C:9]1[C:8]2[N:7]=[C:6]([CH2:19][CH2:20][O:21][CH3:22])[N:5]([CH2:4][C:3]([CH3:24])([CH3:23])[CH2:2][NH:1][C:32]([NH:31][C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)=[O:33])[C:17]=2[C:16]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[N:10]=1

Participants

3

Procedure

Using the general method of Example 145, 1-(3-amino-2,2-dimethylpropyl)-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine (1.0 g, 3.05 mmol) was reacted with phenyl isocyanate to provide 0.45 g of N-(3-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-2,2-dimethylpropyl)-N′-phenylurea as a white powder, m.p. 125.0-130.0° C. Analysis: Calculated for C25H30N6O2. 0.40H2O: %C, 66.18; %H, 6.84; %N, 18.52; Found: %C, 66.05; %H, 6.61; %N, 18.64. %H2O calculated: 1.59; found: 1.53 (Karl Fisher);

Sources & evidence

ORD record
ord-10e81a8c04b24c83958354216e59e43f
Source dataset
uspto-grants-2004_08
Patent number
US06784188B2

Reaction notes

Loading…