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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1412535Generated: November 2, 2026

Ethyl Acetate → HCID 178438719, compound

https://huagongshe.com/reaction/1412535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHCID 178418573HCID 178418573—
ReactantHCID 178438732HCID 178438732—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178438719HCID 17843871988%

Reaction Steps

To a solution of ethyl[(trans-4-{6-[(2′-cyano-3-fluorobiphenyl-4-yl)methyl]-5-oxo-7-propylpyrazolo[1,5-a]pyrimidin-4(5H)-yl}cyclohexyl)oxy]acetate (0.40 g) in tetrahydrofuran (4 mL) was added dropwise methylmagnesium bromide (1 M tetrahydrofuran solution, 0.71 mL) at 0° C., and the mixture was stirred for 30 min. 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 (0.26 g, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921379B2
Source datasetuspto-grants-2014_12
ORD IDord-0941991ba94e4d049951ff86313c25f4
Source noteuspto-grants-2014_12