Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1412468Generated: October 31, 2026

HCID 178420675, compound → HCID 178438634, compound

https://huagongshe.com/reaction/1412468

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178420675HCID 178420675—
ReactantHCID 178438656HCID 178438656—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium ChlorideHCID 25517—
ProductHCID 178438634HCID 178438634—

Reaction Steps

To a solution of 4′-({5-oxo-4-[trans-4-(2-oxoethoxy)cyclohexyl]-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrile (841 mg) in tetrahydrofuran (15 mL) was added 1 M methylmagnesium bromide-tetrahydrofuran solution (2.2 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 basic silica gel chromatography [eluent: hexane/ethyl acetate=70/30→40/60 (volume ratio)] to give the title compound as a colorless amorphous compound (387 mg, 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921379B2
Source datasetuspto-grants-2014_12
ORD IDord-df36e9c3fb8e43d888a55ae0a5360b35
Source noteuspto-grants-2014_12