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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519783Generated: October 29, 2026

HCID 178420675, compound → HCID 178438736, compound

https://huagongshe.com/reaction/519783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178420675HCID 178420675—
ReactantHCID 178438739HCID 178438739—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 178438736HCID 178438736—

Reaction Steps

To a solution of 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}-N-methoxy-N-methylcyclobutanecarboxamide (1.90 g) in tetrahydrofuran (5 mL) was added 1 M methylmagnesium bromide-tetrahydrofuran solution (5.3 mL), and the mixture was stirred at room temperature for 3 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=70/30→50/50 (volume ratio)] to give the title compound as a colorless amorphous compound (1.38 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115136B2
Source datasetuspto-grants-2015_08
ORD IDord-8c1fe035a446486882e310f56a955ec5
Source noteuspto-grants-2015_08