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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1900177Generated: October 25, 2026

Water → N1-[2-(4-cyanophenoxy)-1-methylethyl]-N2-phenoxythiocarbonyl-L-valinamide

https://huagongshe.com/reaction/1900177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-MethylmorpholineHCID 7972—
ReactantPhenyl thioxochloroformateHCID 70498—
ReactantN1-[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamideHCID 22866848—
SolventDichloromethaneHCID 6344—
ProductN1-[2-(4-cyanophenoxy)-1-methylethyl]-N2-phenoxythiocarbonyl-L-valinamideHCID 5417614975%

Reaction Steps

0.4 g of N-methyhnorpholine was added to a suspension containing 1.1 g of N1 -[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamide suspended in 40 ml of methylene chloride, at -15° C. After 0.7 g of phenyl chlorothionoformate was added to the mixture at -15° C., the reaction mixture was allowed to sit and warm naturally to room temperature while being stirred, and was stirred for 15 hours at room temperature. Water was subsequently added to the reaction mixture. After the methylene chloride layer was washed with water, the organic layer was dried over anhydrous magnesium sulfate and the methylene chloride was removed under reduced pressure. The residue was purified by column chromatography on silica gel, thus obtaining 1.2 g of the desired product in the form of a yellow glutinous substance (yield: 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05574064
Source datasetuspto-grants-1996_11
ORD IDord-1898cc8362be43a890087bf1f6bb60cd
Source noteuspto-grants-1996_11