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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480312Generated: November 2, 2026

Hydrogen Peroxide → HCID 90203915, compound

https://huagongshe.com/reaction/1480312

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 90214939HCID 90214939—
SolventEthanolHCID 702—
ProductHCID 90203915HCID 90203915—

Reaction Steps

To a solution of N-[cyano-(3-methyloxetan-3-yl)methyl]-5-cyclopropyl-4-[(1S)-2,2,2-trifluoro-1-methyl-ethoxy]pyridine-2-carboxamide (example 251c, 0.17 g, 443 μmol) in ethanol (3 ml) was added a 4M aqueous solution of sodium hydroxide (554 μl, 2.22 mmol) and H2O2 35% aqueous solution (215 mg, 190 μl, 2.22 mmol). The reaction mixture was stirred at room temperature overnight. The reaction was then concentrated in vacuo and diluted with ethyl acetate. The organic phase was extracted with a 1M aqueous solution of sodium bicarbonate. The organic phase was collected and the aqueous phase was back-extracted with ethyl acetate. The combined organic phases were dried over sodium sulfate and evaporated down to dryness. The crude material was purified by flash chromatography on silica eluting with a heptane-ethyl acetate gradient to yield the mixture of epimers which was then separated into its individual epimers by preparative chiral HPLC (Chiralpak AD, ethanol/heptane) and the title compound was the second epimer collected and isolated as colorless oil; MS (ESI, m/z): 402.6 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409866B2
Source datasetuspto-grants-2016_08
ORD IDord-8009fe9a40d3424fa1d49581d859b521
Source noteuspto-grants-2016_08