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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881499Generated: November 1, 2026

Ammonium Acetate → HCID 178442426, compound

https://huagongshe.com/reaction/1881499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantTert-butyl 2-{[(4,4-dimethyl-2-oxohexyl)amino]carbonyl}-4,4-difluoro-2-[4-(5-fluoropyridin-2-yl)benzyl]pyrrolidine-1-carboxylateHCID 66705635—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 178442426HCID 178442426—

Reaction Conditions

Temperature160 °C

Reaction Steps

Ammonium acetate (947 mg, 12.3 mmol) was added to an ambient temperature solution of tert-butyl 2-{[(4,4-dimethyl-2-oxohexyl)amino]carbonyl}-4,4-difluoro-2-[4-(5-fluoropyridin-2-yl)benzyl]pyrrolidine-1-carboxylate (138 mg, 0.25 mmol) in xylenes (10 mL). After stirring in a sealed tube at 160° C. for 1 h, the reaction mixture was diluted with ethyl acetate and water. The organic phase was dried (magnesium sulfate), filtered, and concentrated in vacuo. The residue was purified by chromatography over silica eluting with 0-100% ethyl acetate/hexane followed by high pressure liquid chromatography (KR100-5C18 100×21.2 mm column) eluting with 10-100% acetonitrile/water containing 0.05% trifluoroacetic acid. The residue was dissolved in trifluoroacetic acid (1 mL). After stirring at ambient temperature for 2 h, the reaction mixture was concentrated to afford the title compound. (M+H) found: 443.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318767B2
Source datasetuspto-grants-2012_11
ORD IDord-d33fcb74c5b843cd9f095a222ca92d91
Source noteuspto-grants-2012_11