Propyl Isothiocyanate → HCID 22479007, compound

HRID 1368145Notes

Reaction equation

HRID 1368145 reaction equation
[NH2:1][CH2:2][CH2:3][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].[CH2:23]([N:26]=[C:27]=[S:28])[CH2:24][CH3:25]>>[NH2:18][C:9]1[C:8]2[N:7]=[C:6]([CH2:19][CH2:20][O:21][CH3:22])[N:5]([CH2:4][CH2:3][CH2:2][NH:1][C:27]([NH:26][CH2:23][CH2:24][CH3:25])=[S:28])[C:17]=2[C:16]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[N:10]=1

Participants

3

Reactant 2

HCID 69403Propyl IsothiocyanateHCID 223444281-(3-aminopropyl)-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine

Product 1

HCID 22479007HCID 22479007, compoundYield 46.4%

Procedure

Using the general method of Example 149, 1-(3-aminopropyl)-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine (1.53 g, 5.11 mmol) was reacted with propyl isothiocyanate (570 mg, 5.62 mmol) to provide 950 mg of N-{3-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]propyl}N′-propylthiourea as a tan powder, m.p. 172-173° C. Analysis: Calculated for C20H28N6OS: %C, 59.97; %H, 7.05; %N, 20.98; Found: %C, 59.83; %H, 7.01; %N, 20.95.

Sources & evidence

ORD record
ord-c50ceaa5eff04fa6942ddd110f3c7601
Source dataset
uspto-grants-2003_06
Patent number
US06573273B1

Reaction notes

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