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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1845717Generated: November 2, 2026

Trifluoroacetic acid → HCID 57568671, compound

https://huagongshe.com/reaction/1845717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 68923284HCID 68923284—
SolventDichloromethaneHCID 6344—
ProductHCID 57568671HCID 5756867153%

Reaction Steps

A solution of tert-butyl 2-[4-({2-[4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-1,1-dimethylethyl}amino)-4-oxobutanoyl]hydrazinecarboxylate (792 mg, 1.50 mmol) in dichloromethane (30 mL) was treated with trifluoroacetic acid (3 mL). After stirring for 2 hours, additional trifluoroacetic acid (3 mL) was added to the reaction mixture and stirring was continued for 1 hour. The reaction mixture was concentrated under reduced pressure and the resulting syrup was dissolved in water. The solution was made basic by the addition of concentrated ammonium hydroxide and then was extracted repeatedly with 10% methanol/chloroform. The combined organic portions were dried over sodium sulfate, filtered, and concentrated under reduced pressure. The crude white solid was purified by chromatography on silica gel (gradient elution, 25%-75% CMA in chloroform) gave 340 mg of N-{2-[4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]-1,1-dimethylethyl}-4-hydrazino-4-oxobutanamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08951528B2
Source datasetuspto-grants-2015_02
ORD IDord-024a38d4f8df407aaf91c71d9d6a9578
Source noteuspto-grants-2015_02