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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045831Generated: October 26, 2026

4-Methylmorpholine → HCID 86672690, compound

https://huagongshe.com/reaction/1045831

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl chloroformateHCID 10928—
ReactantN-Methyl-N-nitrosoureaHCID 12699—
ReactantPotassium HydroxideHCID 14797—
Reactant(R)-2-BOC-amino-3-(4-methoxy-benzylsulfanyl)-propionic acidHCID 68486000—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 86672690HCID 8667269095%

Reaction Conditions

Temperature-25 °C

Reaction Steps

(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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569307B2
Source datasetuspto-grants-2013_10
ORD IDord-b6b97ee36179453e8217929be77c195f
Source noteuspto-grants-2013_10