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HRID 538921作成日:2026年10月24日

4-Methylmorpholine → Phenylmethyl (3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutanoate

https://huagongshe.com/ja/reaction/538921

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Isobutyl chloroformateHCID 62365—
反応物N-tert-Butoxycarbonyl-L-aspartic acid beta-benzyl esterHCID 1581888—
反応物Sodium borohydrideHCID 4311764—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物Phenylmethyl (3S)-3-[[(1,1-dimethylethoxy)carbonyl]amino]-4-hydroxybutanoateHCID 10040985—

反応条件

温度-20 °C

反応手順

To a solution of Boc-L-aspartic acid-4-benzyl ester (100 g, 309 mmol) in DME (1.8 L) at −20° C. was added NMM (34 mL, 309 mmol) then dropwise iso-butylchloroformate (40 mL, 309 mmol) and the mixture was stirred at −20° C. for 20 min. The reaction mixture was filtered and the filtrate was cooled to −20° C. NaBH4 (17.5 g, 463 mmol) was added portionwise at −20° C. The mixture was allowed to warm and stirred at rt for 1 h. The mixture was quenched with a 20% citric acid solution and then extracted with AcOEt. The organic layer was washed with NaHCO3 solution, H2O and brine, dried (MgSO4), filtered and concentrated. The product was used without further purification for the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08865894B2
出典データセットuspto-grants-2014_10
ORD IDord-379a98ce8165465aad03657a829ab132
出典メモuspto-grants-2014_10