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HRID 340950作成日:2026年10月23日

Formaldehyde → (S)-benzyl 4-(3-(1,3-dioxoisoindolin-2-yl)propyl)-5-oxooxazolidine-3-carboxylate

https://huagongshe.com/ja/reaction/340950

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物p-Toluenesulfonic acidHCID 6101—
反応物N-CarbethoxyphthalimideHCID 31187—
反応物N-alpha-Benzyloxycarbonyl-L-ornithineHCID 7010490—
溶媒TolueneHCID 1140—
溶媒Diethyl EtherHCID 3283—
溶媒Ethyl AcetateHCID 8857—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物(S)-benzyl 4-(3-(1,3-dioxoisoindolin-2-yl)propyl)-5-oxooxazolidine-3-carboxylateHCID 5438015676%

反応条件

温度150 °C

反応手順

(S)-5-amino-2-(benzyloxycarbonylamino)pentanoic acid (10.0 g, 37.56 mmol) and ethyl 1,3-dioxoisoindoline-2-carboxylate (9.04 g, 41.28 mmol) in NMP (40.0 mL) were heated to 150° C. for 30 min in 4 microwave reaction tubes. The mixture was diluted with EtOAc (500 mL). The organic mixture was washed with water (100 mL×2) and brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to give an oil, which was redissolved in toluene. To the resulting solution were added paraformaldehyde, PTSA and molecular sieves (3 A) and the mixture was heated to 150° C. for 20 min in a microwave reactor. The reaction mixture was diluted with ether (800 mL), washed with NaHCO3 and brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified on silica gel using a mixture of EtOAc and hexanes to give (S)-benzyl 4-(3-(1,3-dioxoisoindolin-2-yl)propyl)-5-oxooxazolidine-3-carboxylate (11.6 g, 76% for 2 steps).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895582B2
出典データセットuspto-grants-2014_11
ORD IDord-7b98d7b8016e43bab56041ff2c72cb2e
出典メモuspto-grants-2014_11