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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585139Generated: November 1, 2026

Sodium borohydride → HCID 22339372, compound

https://huagongshe.com/reaction/585139

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22339619HCID 22339619—
SolventMethanolHCID 887—
ProductHCID 22339372HCID 22339372—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.), stirred solution of 2-{3-chloro-4-[3-(4-fluoro-benzoyl)-4-hydroxy-phenoxy]-5-methyl-phenyl}-2H-[1,2,4]triazine-3,5-dione (0.4 g) in methanol (10 mL) was added sodium borohydride (32 mg). After 30 min, the reaction solution was concentrated in vacuo, partitioned between 1N hydrochloric acid and ethyl acetate, the organic phase dried (Na2SO4), concentrated in vacuo and flash chromatographed on silica gel (5% ethanol/dichloromethane) to afford the title compound of Step C as a colorless foam, 72 mg. MS Calc.:469.8; Found:467.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06930107B2
Source datasetuspto-grants-2005_08
ORD IDord-21baca2cdefd457f9bfd3a0e092b4a09
Source noteuspto-grants-2005_08