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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 442758생성일: 2026년 10월 27일

Triethylamine → (4R)-N-[(1S)-1-Methyl-2-hydroxyethyl]-2-oxothiazolidin-4-yl-carboxamide

https://huagongshe.com/reaction/442758

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물ProcysteineHCID 72390—
반응물L-AlaninolHCID 80307—
반응물P,P-Diphenylphosphinic azideHCID 199401—
용매TetrahydrofuranHCID 8028—
생성물(4R)-N-[(1S)-1-Methyl-2-hydroxyethyl]-2-oxothiazolidin-4-yl-carboxamideHCID 2130914066.3%

반응 단계

In 20 ml of dry tetrahydrofuran were dissolved 1.0 g of (4R)-2-oxothiazolidine-4-carboxylic acid and 0.56 g of L-alaninol, 2.8 ml of triethylamine and 1.8 ml of diphenylphosphoryl azide were added thereto with stirring under ice-cooling, and the mixture was stirred at room temperature for 3 hours. Then, the solvent was distilled off under reduced pressure and the obtained residue was purified by silica gel column chromatography employing ethyl acetate as an eluent and further purified by silica gel column chromatography employing dichloromethane-methanol (95:5) as an eluent to obtain 0.92 g of the desired compound as colorless crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05891898
출처 데이터셋uspto-grants-1999_04
ORD IDord-91ff4ee8f9bc4b65ad9810482c255100
출처 메모uspto-grants-1999_04