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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048498Generated: November 1, 2026

HCID 178420675, compound → HCID 178438623, compound

https://huagongshe.com/reaction/2048498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178420675HCID 178420675—
ReactantHCID 178438633HCID 178438633—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 178438623HCID 178438623—

Reaction Steps

To a solution of 4′-({5-oxo-4-[trans-4-(2-oxopropoxy)cyclohexyl]-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrile (251 mg) in tetrahydrofuran (3 mL) was added 1 M methylmagnesium bromide-tetrahydrofuran solution (1 mL), and the mixture was stirred at room temperature for 16 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 basic silica gel chromatography [eluent: hexane/ethyl acetate=70/30→40/60 (volume ratio)] to give the title compound as a colorless amorphous compound (237 mg, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592431B2
Source datasetuspto-grants-2013_11
ORD IDord-2eda21000651469c99e24680e8c7d69a
Source noteuspto-grants-2013_11