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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1412235Generated: November 2, 2026

HCID 178418573, compound → HCID 178438718, compound

https://huagongshe.com/reaction/1412235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178418573HCID 178418573—
ReactantHCID 178438729HCID 178438729—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178438718HCID 178438718—

Reaction Steps

tert-Butyl 2-[(trans-4-{6-[(2′-cyano-3-fluorobiphenyl-4-yl)methyl]-5-oxo-7-propyl[1,2,4]triazolo[1,5-a]pyrimidin-4(5H)-yl}cyclohexyl)oxy]propanoate (548 g) was dissolved in tetrahydrofuran (2.7 L), and methylmagnesium bromide (1.0 M tetrahydrofuran solution, 3.5 L) was added with the internal temperature maintained below 10° C. The reaction mixture was stirred at the same temperature for 1 hr, and partitioned among saturated aqueous ammonium chloride solution (600 mL), water (600 mL) and ethyl acetate (500 mL). The aqueous layer was extracted with ethyl acetate (1 L). The combined extracts were washed with saturated brine (1 L), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to give the title compound as a racemate (428 g, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921379B2
Source datasetuspto-grants-2014_12
ORD IDord-44c3afdf48b544609958d552f36d3eba
Source noteuspto-grants-2014_12