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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047237Generated: October 30, 2026

Trifluoroacetic acid → HCID 86696617, compound

https://huagongshe.com/reaction/1047237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86696616HCID 86696616—
SolventMethanolHCID 887—
ProductHCID 86696617HCID 8669661758.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of ethyl 2-(5-bromo-3-(isopropylamino)pyrazin-2-ylamino)acetate (780 mg, 2.26 mmol), methanol (5 mL) and TFA (10 mL) in a sealable vessel was purged with nitrogen, sealed, stirred vigorously and heated at 90° C. with an oil bath for 16 h. The resulting mixture was diluted with methanol and the solvent was removed under reduced pressure. Methanol (10 mL) was added and the solvent was removed under reduced pressure again. Methanol (10 mL) and sodium bicarbonate were added. The resulting mixture was stirred at room temperature until pH=6 (in water), the solvent was removed under reduced pressure. Water (20 mL) was added. The mixture was extracted with methylene chloride (20 mL×3). The organic layer was dried over anhydrous sodium sulfate, concentrated to give the crude product and purified on silica column chromatography (10-20% ethyl acetate in petroleum ether) to give the title compound (360 mg, 39.4% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569494B2
Source datasetuspto-grants-2013_10
ORD IDord-8b1076ae0a074e4cb4986d6e72fdfeba
Source noteuspto-grants-2013_10