Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055946Generated: November 1, 2026

Sodium borohydride → HCID 10249539, compound

https://huagongshe.com/reaction/2055946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 10452578HCID 10452578—
SolventEthanolHCID 702—
ProductHCID 10249539HCID 10249539—

Reaction Steps

The title compound was prepared analogous to the methods used in Example 33 using 5-[6-(4-trifluoromethyl-phenyl)-pyrimidin-4-yloxy]-1H-quinoxalin-2-one, (Example 34(b)), (0.25 g, 0.65 mmol) and sodium borohydride (0.11 mg, 2.8 mmol, Aldrich) in EtOH (5 mL). 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-10bc38f47e1b4f79bd5db6d1258f8ff8
Source noteuspto-grants-2008_02