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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 336445생성일: 2026년 10월 24일

4-Methylmorpholine → HCID 86672690, 화합물

https://huagongshe.com/ko/reaction/336445

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물TetrahydrofuranHCID 8028—
반응물Ethyl chloroformateHCID 10928—
반응물N-Methyl-N-nitrosoureaHCID 12699—
반응물Potassium HydroxideHCID 14797—
반응물(R)-2-BOC-amino-3-(4-methoxy-benzylsulfanyl)-propionic acidHCID 68486000—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
생성물HCID 86672690HCID 8667269095%

반응 조건

온도-25 °C

반응 단계

(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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889691B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-81b1320c0299424cbca1f3cbf17faa69
출처 메모uspto-grants-2014_11