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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26318생성일: 2026년 10월 24일

Triethylamine → 3-(Acetyloxy)methyl-7-[[4-(1-pyrryl)butyryl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]-oct-2-ene-2-carboxylic acid

https://huagongshe.com/ko/reaction/26318

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3-((Acetyloxy)methyl)-7-amino-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-2-carboxylic acidHCID 13729—
반응물Isobutyl chloroformateHCID 62365—
반응물4-(1H-pyrrol-1-yl)butanoic acidHCID 10419380—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물3-(Acetyloxy)methyl-7-[[4-(1-pyrryl)butyryl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]-oct-2-ene-2-carboxylic acidHCID 70605273—

반응 조건

온도-10 °C

반응 단계

4-(1-Pyrryl)butanoic acid (0.05 mole) is dissolved in 50 ml of tetrahydrofuran (THF) and 0.05 mole of triethylamine is added. This mixture is cooled to -10° C. and 0.05 mole of isobutylchloroformate is added. The mixture is stirred for 0.5 hours at -5° C. and then 0.05 mole of 3-[(acetyloxy)methyl]-7-amino-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid and 0.075 mole of triethyl amine in 50 ml of THF (precooled) is added. The mixture is stirred at 0° C. for 1 hour and then warmed to room temperature. The mixture is diluted with water and extracted with ethyl acetate. The aqueous layer is acidified and extracted with ethyl acetate. The ethyl acetate extracts are combined, dried, filtered, and the solvent evaporated to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04148998
출처 데이터셋uspto-grants-1979_04
ORD IDord-6631c8a00d354e8eb16797c3c5063d19
출처 메모uspto-grants-1979_04