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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207986Generated: October 31, 2026

Sodium borohydride → HCID 118432152, compound

https://huagongshe.com/reaction/2207986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 118431627HCID 118431627—
SolventMethanolHCID 887—
ProductHCID 118432152HCID 11843215285.9%

Reaction Steps

5-(4′-Acetyl-biphenyl-3-yl)-1-(2-chloro-phenyl)-3-pentafluoroethyl-4,5-dihydro-1H-pyrazole (18.0 mg, 0.04 mmol) prepared in Example 107 and sodium borohydride (2.0 mg, 0.06 mmol) were added at 0° C. to methanol (2.0 mL). The reaction mixture was stirred at room temperature for 3 hours, quenched with distilled water, 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 17.0 mg of the titled compound as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376420B2
Source datasetuspto-grants-2016_06
ORD IDord-c37e63e0c9854eabadb75c5caf0f3736
Source noteuspto-grants-2016_06