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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1087076생성일: 2026년 10월 26일

Water → cis-(+-)-N-(2-(2,6-Dimethyl-1-piperidinyl)ethyl)-2-oxo-3-hydroxy-1-pyrrolidineacetamide

https://huagongshe.com/reaction/1087076

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물2-(cis-2,6-Dimethyl-1-piperidinyl)ethanamineHCID 783702—
반응물(R/S)-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)acetic acidHCID 19817647—
용매DimethylformamideHCID 6228—
생성물cis-(+-)-N-(2-(2,6-Dimethyl-1-piperidinyl)ethyl)-2-oxo-3-hydroxy-1-pyrrolidineacetamideHCID 3069833—

반응 단계

1.30 g of dicyclohexylcarbodiimide dissolved in 6 ml of dimethylformamide are added dropwise at 0° to 1.0 g of (R/S)-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)acetic acid and 1.03 g of 94.7% cis-2-(2,6-dimethyl-1-piperidinyl)ethylamine dissolved in 20 ml of dimethylformamide. The mixture is left to stirred at room temperature for 4 days, treated with 0.23 of ion-free water and evaporated in a water-jet vacuum. The residue is treated five times with toluene and is each case again evaporated. The constituents of the residue which are soluble in chloroform are chromatographed on 60 g of aluminum oxide (activity grade III, neutral). The alcohol eluate is again chromatographed on 15 g of aluminum oxide (activity grade III, neutral). The fractions which are eluted with acetonitrile and ethanol contain, according to the gas chromatogram and mass spectrum, (R/S)-cis-N-[2-(2,6-dimethyl-1-piperidinyl)ethyl]-2-(3-hydroxy-2-oxo-1-pyrrolidinyl)acetamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05034402
출처 데이터셋uspto-grants-1991_07
ORD IDord-24c9d2a257e9495e8f6beb1189a40c25
출처 메모uspto-grants-1991_07