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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006216Generated: November 1, 2026

Sodium borohydride → HCID 22339372, compound

https://huagongshe.com/reaction/1006216

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 numberUS06787652B1
Source datasetuspto-grants-2004_09
ORD IDord-68b3cde8893e4d5db4371420249f874b
Source noteuspto-grants-2004_09