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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707300Generated: October 30, 2026

Trifluoroacetic acid → HCID 178454115, compound

https://huagongshe.com/reaction/707300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantPotassium CarbonateHCID 11430—
Reactant4,6-Dichloro-5-nitropyrimidineHCID 20312—
ReactantHCID 178454113HCID 178454113—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178454115HCID 178454115—

Reaction Steps

Tert-butyl(trans-3-(quinazolin-2-ylamino)cyclobutyl)carbamate, which was synthesized analagous to intermediate 10, (1.71 g, 5.44 mmol) was dissolved in dichloromethane (20 mL) and treated with trifluoroacetic acid (5 mL). The solution was stirred at room temperature for 20 minutes after which the solution was evaporated to dryness under reduced pressure. The crude oil was further dried under high vacuum then dissolved in dry dimethylsulfoxide (40 mL). 4,6-Dichloro-5-nitropyrimidine (1.5 g, 7.73 mmol) was added followed by potassium carbonate (1.8 g, 13.02 mmol) and the reaction heated at 60° C. After 2 hours the mixture was cooled and diluted with water (300 mL). The product precipitated out and was filtered off using a sintered glass frit. It was dried on the frit and used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174992B2
Source datasetuspto-grants-2015_11
ORD IDord-dc55885562424cc7a49582f2b0d7651c
Source noteuspto-grants-2015_11