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HRID 393562作成日:2026年10月26日

4-Methylmorpholine → Tert-butyl N-[(3S)-1-bromo-5-methyl-2-oxohexan-3-YL]carbamate

https://huagongshe.com/reaction/393562

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DiazomethaneHCID 9550—
反応物L-Leucine, N-((1,1-dimethylethoxy)carbonyl)-HCID 83170—
反応物2-Chloroethyl formateHCID 246748—
反応物Acetic Acid Mixture with Hydrobromic AcidHCID 21893785—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物Tert-butyl N-[(3S)-1-bromo-5-methyl-2-oxohexan-3-YL]carbamateHCID 11034179—

反応手順

Under atmosphere of argon, to a solution of (2S)-2-(t-butoxycarbonylamino)-4-methylpentanoic acid (t-butoxycarbonyl-L-leucine) (37.4 g) in tetrahydrofuran (800 ml) was added N-methylmorpholine (33 ml) at −25° C. and the mixture was stirred for 10 minutes. To the mixture was added chloroethylformate (15.8 ml) and the mixture was stirred for 20 minutes. Thereto was added a solution of diazomethane in diethyl ether and the mixture was stirred for another 2 hours. Thereto was added a mixture of 47% hydrobromic acid-acetic acid (1:1) at 0° C. and the mixture was stirred for 15 minutes. To the reaction mixture was added water and was extracted with a mixture of ethyl acetate-hexane. The organic layer was washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride successively, dried over anhydrous sodium sulfate and was concentrated. The residue was washed with cooled hexane to give the title compound (27.4 g) having the following physical data.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06809092B2
出典データセットuspto-grants-2004_10
ORD IDord-a70f5ebccb964f229b26a4b36f6d4754
出典メモuspto-grants-2004_10