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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1688752Generated: October 30, 2026

HCID 178420675, compound → HCID 178438749, compound

https://huagongshe.com/reaction/1688752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178420675HCID 178420675—
ReactantHCID 178438754HCID 178438754—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 178438749HCID 178438749—

Reaction Steps

To a solution of ethyl [(trans-3-{6-[(2′-cyano-3-fluorobiphenyl-4-yl)methyl]-2-methyl-5-oxo-7-propyl[1,2,4]triazolo[1,5-a]pyrimidin-4(5H)-yl}cyclobutyl)oxy]acetate (557 mg) in tetrahydrofuran (5 mL) was added 1 M methylmagnesium bromide-tetrahydrofuran solution (5 mL), and the mixture was stirred at room temperature for 15 hr. The reaction mixture was diluted with saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography [eluent: hexane/ethyl acetate=65/35→40/60 (volume ratio)] to give the title compound as a colorless amorphous compound (437 mg, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148383B2
Source datasetuspto-grants-2012_04
ORD IDord-898ca6984f514fa7a2f6b2c237e30aee
Source noteuspto-grants-2012_04