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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1900178Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/1900178

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4-MethylmorpholineHCID 7972—
EduktPhenyl ChlorodithioformateHCID 592675—
EduktN1-[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamideHCID 22866848—
LösungsmittelDichloromethaneHCID 6344—
ProduktN1-[2-(4-cyanophenoxy)-1-methylethyl]-N2-(phenylthio)thiocarbonyl-L-valinamideHCID 5387387368,6%

Reaktionsschritte

0.5 g of N-methylmorpholine was added to a suspension containing 1.4 g of N1 -[2-(4-cyanophenoxy)-1-methylethyl]-L-valinamide suspended in 40 ml of methylene chloride, at -15° C. After 0.9 g of phenyl chlorodithioformate 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 1.4 g of the desired product in the form of a yellow glutinous substance (yield: 66%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05574064
Quelldatensatzuspto-grants-1996_11
ORD IDord-379fa347b45b4d9b9dd21b027bd28161
Quellennotizuspto-grants-1996_11