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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1412545Generated: November 2, 2026

Ethyl Acetate → HCID 178440649, compound

https://huagongshe.com/reaction/1412545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantHCID 178418573HCID 178418573—
ReactantHCID 178440650HCID 178440650—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178440649HCID 17844064963%

Reaction Steps

To a solution of ethyl({trans-4-[7-butyl-6-{[6-(2-cyanophenyl)pyridin-3-yl]methyl}-5-oxopyrazolo[1,5-a]pyrimidin-4(5H)-yl]cyclohexyl}oxy)acetate (0.26 g) in tetrahydrofuran (3 mL) was added dropwise methylmagnesium bromide (1 M tetrahydrofuran solution, 1.4 mL) at 0° C., and the mixture was stirred for 3 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 (0.16 g, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921379B2
Source datasetuspto-grants-2014_12
ORD IDord-bef9cef48ad445eabe40a3dfbd7a5107
Source noteuspto-grants-2014_12