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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207975Generated: October 31, 2026

Sodium borohydride → HCID 118431962, compound

https://huagongshe.com/reaction/2207975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 118432063HCID 118432063—
SolventEthanolHCID 702—
ProductHCID 118431962HCID 118431962—

Reaction Steps

To a solution of 1-(2,4-difluoro-phenyl)-5-(3-(3-formyl-2-methoxy-pyridin-5-yl)-phenyl)-3-pentafluoroethyl-4,5-dihydro-1H-pyrazole (20 mg, 0.04 mmol) prepared in Example 73 in ethanol (1 mL), was slowly added sodium borohydride (6.0 mg, 0.16 mmol) at 0° C. The reaction mixture was stirred at room temperature for 1 hour, quenched with a 1N hydrochloric acid solution, and then extracted with ethyl acetate three times. The combined extract was washed with brine, dried on anhydrous magnesium sulfate, and then concentrated under reduced pressure to give a residue as a pale yellow liquid. The resulting residue was purified by silica gel column chromatography (eluent: ethyl acetate/n-hexane=2/1) to give 3.0 mg of the titled compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376420B2
Source datasetuspto-grants-2016_06
ORD IDord-b0533fb45d62429b9b97ae2197bb3c69
Source noteuspto-grants-2016_06