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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2048557Generated: October 31, 2026

Ethyl Acetate → HCID 178438629, compound

https://huagongshe.com/reaction/2048557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHCID 178418630HCID 178418630—
ReactantHCID 178438630HCID 178438630—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178438629HCID 17843862968%

Reaction Steps

To a solution of 4′-({5-oxo-4-[trans-4-(2-oxopropoxy)cyclohexyl]-7-propyl-4,5-dihydropyrazolo[1,5-a]pyrimidin-6-yl}methyl)biphenyl-2-carbonitrile (0.30 g) in tetrahydrofuran (3 mL) was added dropwise cyclopropylmagnesium bromide (0.5M tetrahydrofuran solution, 2.3 mL) at 0° C., and the mixture was stirred for 2 hr. To the reaction mixture were added ethyl acetate and then saturated aqueous ammonium chloride solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated. The residue was purified by silica gel column chromatography to give the title compound as a pale-yellow amorphous solid (0.22 g, 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592431B2
Source datasetuspto-grants-2013_11
ORD IDord-ea8071d12cc74541b7b4ca3a63e9cecf
Source noteuspto-grants-2013_11