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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105492Generated: November 3, 2026

Trichloroacetyl isocyanate → HCID 57538842, compound

https://huagongshe.com/reaction/2105492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetyl isocyanateHCID 76400—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 67506136HCID 67506136—
ProductHCID 57538842HCID 5753884228%

Reaction Steps

The methods described in Parts C and D of Example 20 were used to oxidize and aminate 2-butyl-1-methoxy-1H-imidazo[4,5-c]quinoline (3.2 g, 12.5 mmol) with the following modifications. The oxidation reaction was stirred for two hours at room temperature. The reaction with trichloroacetyl isocyanate (2.2 mL, 19 mmol) was carried out at room temperature overnight, and the reaction sodium methoxide was stirred overnight and then concentrated under reduced pressure. The residue was treated with methanol (5 mL) to form a solid, which was collected by filtration and recrystallized from methanol/water and dried overnight in a vacuum oven at 70° C. to provide 0.946 g of 2-butyl-1-methoxy-1H-imidazo[4,5-c]quinolin-4-amine as golden crystals, mp 197-199° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579359B2
Source datasetuspto-grants-2009_08
ORD IDord-969789d85d4b49b3a91f454b55873da7
Source noteuspto-grants-2009_08