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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 484675생성일: 2026년 10월 25일

Dicyclohexylcarbodiimide → (3S-trans)-3-[[[[(4-Ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]phenylacetyl]amino]-4-methyl-1-(phenylmethoxy)-2-azetidinone

https://huagongshe.com/reaction/484675

반응식

참여 물질

역할이름HCID투입량
반응물DicyclohexylcarbodiimideHCID 10868—
반응물DiisopropylethylamineHCID 81531—
반응물ToluenesulfonateHCID 3424274—
반응물(R)-(-)-alpha-[[(4-Ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]benzeneacetic acidHCID 4550893—
반응물(3S-trans)-3-amino-4-methyl-1-(phenylmethoxy)-2-azetidinoneHCID 13036842—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물(3S-trans)-3-[[[[(4-Ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]phenylacetyl]amino]-4-methyl-1-(phenylmethoxy)-2-azetidinoneHCID 13036845—

반응 단계

A suspension of α-[[(4-ethyl-2,3-dioxo-1-piperazinyl)carbonyl]amino]benzeneacetic acid (0.879 g) hydroxybenzotriazole (0.42 g), and dicyclohexylcarbodiimide (0.56 g), in dimethylformamide (15 ml) is stirred at 26° C. for one hour, at which point a solution of (3S-trans)-3-amino-4-methyl-1-(phenylmethoxy)-2-azetidinone, toluenesulfonate (0.95 g) and diisopropylethylamine (0.44 ml) in dimethylformamide (5 ml) is added. The reaction mixture is stirred at room temperature for about 16 hours, then poured into water (100 ml) and extracted with ethyl acetate (three 100 ml portions). The combined organic extracts are washed with water (three 100 ml portions) and aqueous sodium bicarbonate solution (one 100 ml portion), then dried over sodium sulfate and concentrated under reduced pressure to a semi-solid residue. Liquid chromatography (ethyl acetate) affords the desired product as a foam (0.599 g). Recrystallization from chloroform/isopropyl ether yields the title compound, melting point 100°-105° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04533660
출처 데이터셋uspto-grants-1985_08
ORD IDord-1cd3e7177e15445185e56858cdbd4246
출처 메모uspto-grants-1985_08