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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828178Generated: October 30, 2026

Ethyl Acetate → HCID 22063832, compound

https://huagongshe.com/reaction/1828178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantMethyl morpholine oxideHCID 82029—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22063871HCID 22063871—
CatalystHCID 178419074HCID 178419074—
SolventDichloromethaneHCID 6344—
ProductHCID 22063832HCID 22063832—

Reaction Steps

N-[2-(1-Cyclopentyl-3-methyl-2-oxo-2,3-dihydro-1H-benzoimidazol-5-yl)-2-hydroxy-1-m-tolyl-ethyl]-3-methoxy-propionamide (433 mg, 0.96 mmol) was dissolved in methylene chloride (9.6 mL) and N-methylmorpholine N-oxide (168.7 mg, 1.44 mmol) was added. After stirring for ten minutes, TPAP (20.2 mg, 0.06 mmol) was added. The reaction was stirred for 1 hour, after which time LCMS and TLC (ethyl acetate) indicated complete reaction. The reaction mixture was poured into saturated aqueous sodium bicarbonate and additional methylene chloride was added. The organic phase was separated and washed with brine, followed by aqueous copper sulfate. The organic phase was then filtered through a plug of silica gel, eluting with ethyl acetate. Concentration of the filtrate afforded 294 mg of a white X solid that was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056918B2
Source datasetuspto-grants-2006_06
ORD IDord-9e2ce73698b042c3a996a6ca66856b26
Source noteuspto-grants-2006_06