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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519824Generated: November 1, 2026

Ethyl Acetate → HCID 178438719, compound

https://huagongshe.com/reaction/519824

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 numberUS09115136B2
Source datasetuspto-grants-2015_08
ORD IDord-b381a90c60d54e95ae29feb0c1e5cf95
Source noteuspto-grants-2015_08