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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1045831Erstellt: 26. Oktober 2026

4-Methylmorpholine → HCID 86672690, Verbindung

https://huagongshe.com/reaction/1045831

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktTetrahydrofuranHCID 8028—
EduktEthyl chloroformateHCID 10928—
EduktN-Methyl-N-nitrosoureaHCID 12699—
EduktPotassium HydroxideHCID 14797—
Edukt(R)-2-BOC-amino-3-(4-methoxy-benzylsulfanyl)-propionic acidHCID 68486000—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
ProduktHCID 86672690HCID 8667269095%

Reaktionsbedingungen

Temperatur-25 °C

Reaktionsschritte

(R)-2-BOC-amino-3-(4-methoxy-benzylsulfanyl)-propionic acid (43 g, 132 mmol) prepared in Step B, 1-methylmorpholine (14.5 mL, 132 mmol) and ethylchloroformate (14.1 mL, 132 mmol) were dissolved in tetrahydrofuran (500 mL), and the mixture was stirred for 1 h at −25° C. At the same time, potassium hydroxide (75 g, 1336 mmol) was dissolved in water (75 mL) and diethylether (750 mL), N-methyl-nitrosourea (26 g, 252 mmol) was added in drops thereto over 2 h at 0° C., and the mixture was stirred for 30 min. The two solutions thus obtained were mixed together, and stirred for 3 h at −25° C. to room temperature. After completion of the reaction, water was added to the reaction mixture, which was then washed with saturated aqueous sodium hydrogen carbonate solution and saturated aqueous ammonium chloride solution in the order. The organic layer was concentrated to give the title compound (46.0 g, Yield 95%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08569307B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-b6b97ee36179453e8217929be77c195f
Quellennotizuspto-grants-2013_10