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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717147Generated: October 29, 2026

Trifluoroacetic acid → HCID 86696617, compound

https://huagongshe.com/reaction/717147

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 numberUS09193692B2
Source datasetuspto-grants-2015_11
ORD IDord-c592b1d948674f45aad0a508d2270ab0
Source noteuspto-grants-2015_11