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HRID 336445作成日:2026年10月25日

4-Methylmorpholine → HCID 86672690、化合物

https://huagongshe.com/reaction/336445

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylmorpholineHCID 7972—
反応物TetrahydrofuranHCID 8028—
反応物Ethyl chloroformateHCID 10928—
反応物N-Methyl-N-nitrosoureaHCID 12699—
反応物Potassium HydroxideHCID 14797—
反応物(R)-2-BOC-amino-3-(4-methoxy-benzylsulfanyl)-propionic acidHCID 68486000—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物HCID 86672690HCID 8667269095%

反応条件

温度-25 °C

反応手順

(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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889691B2
出典データセットuspto-grants-2014_11
ORD IDord-81b1320c0299424cbca1f3cbf17faa69
出典メモuspto-grants-2014_11