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HRID 1036738作成日:2026年10月26日

Water → (2R,3S)-3-(Benzyloxy)-2-(2-(tert-butoxycarbonylamino)-2-methylpropanamido)butanoic acid

https://huagongshe.com/reaction/1036738

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物O-Benzyl-D-threonineHCID 22869571—
反応物Tert-butyl 1-(2,5-dioxopyrrolidin-1-yl)-2-methyl-1-oxopropan-2-ylcarbamateHCID 71060486—
溶媒TetrahydrofuranHCID 8028—
生成物(2R,3S)-3-(Benzyloxy)-2-(2-(tert-butoxycarbonylamino)-2-methylpropanamido)butanoic acidHCID 71060529—

反応条件

温度50 °C

反応手順

A mixture comprising of tert-butyl 1-(2,5-dioxopyrrolidin-1-yl)-2-methyl-1-oxopropan-2-ylcarbamate (1 g, 3.33 mmol) (prepared according to the procedure described in EP1486498A1 page 20) and (2R,3S)-2-amino-3-(benzyloxy)butanoic acid (0.697 g, 3.33 mmol) in THF (40 ml)/water (10 ml) was treated with TEA (1.392 ml, 9.99 mmol) and stirred at 50° C. for 4 hours. The resulting mixture was concentrated in vacuo and EtOAc (20 ml) was added. The pH was adjusted to pH2 with 1M HCl. The organic portion was separated and the aqueous phase was back extracted with EtOAc (30 ml). The combined organic portions were washed with a saturated solution of brine (50 ml), dried (MgSO4), filtered and concentrated in vacuo. The residue was dissolved in DCM and concentrated in vacuo to afford the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08546416B2
出典データセットuspto-grants-2013_10
ORD IDord-e4bac0c5cb0548f7a485dab0aeaa5f6d
出典メモuspto-grants-2013_10