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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519834Generated: October 31, 2026

Ethyl Acetate → HCID 178440649, compound

https://huagongshe.com/reaction/519834

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 numberUS09115136B2
Source datasetuspto-grants-2015_08
ORD IDord-429866f1bab44047a53f99259a56a0e6
Source noteuspto-grants-2015_08