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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055945Generated: October 31, 2026

Sodium borohydride → HCID 21865094, compound

https://huagongshe.com/reaction/2055945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21865040HCID 21865040—
SolventEthanolHCID 702—
ProductHCID 21865094HCID 21865094—

Reaction Steps

To a suspension of 8-[6-(4-trifluoromethyl-phenyl)-pyrimidin-4-yloxy]-1H-quinoxalin-2-one, (Example 32(e)), (0.25 g, 0.65 mmol) in EtOH (5 mL) was added sodium borohydride (0.11 mg, 2.8 mmol, Aldrich). After stirring at room temperature for 2 h, the mixture was quenched with satd aq. NaHCO3 and extracted with 25% i-PrOH/CHCl3 (3×). The combined organic layers were dried over Na2SO4, filtered and concentrated. Purification by flash chromatography (0→1.5% 2M NH3/MeOH in CH2Cl2) gave the title compound as a light-yellow powder. Mp: 305° C., MS (ESI, pos. ion) m/z: 387 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07332511B2
Source datasetuspto-grants-2008_02
ORD IDord-0cdc18a165f3473a8ce8ed580cd6aa2b
Source noteuspto-grants-2008_02