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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 341905생성일: 2026년 10월 26일

Hydrochloric Acid → (6R,7R)-7-amino-3-formyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

https://huagongshe.com/reaction/341905

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PyridineHCID 1049—
반응물7-Amino-3-formyl-3-cephem-4-carboxylic acidHCID 87203762—
용매MethanolHCID 887—
생성물(6R,7R)-7-amino-3-formyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 15385898—

반응 단계

2.64 g of the hydrochloride of 6-amino-1,4,5a,6-tetrahydro-3-hydroxy-1,7-dioxo-3H,7H-aceto[2,1-b]furo[3,4-d][1,3]thiazine (hydroxylactone of the hydrochloride of 7-amino-3-formyl-3-cephem-4-carboxylic acid) are dissolved in 50 ml of methanol. A solution of 0.78 g of pyridine in 10 ml of methanol is added dropwise to this solution whilst stirring and cooling with ice. The precipitated product is filtered off under nitrogen whilst excluding moisture, washed with a little methanol and dried over a drying agent in vacuo at room temperature. (6R-trans)-7-amino-3-formyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid is thus obtained in the form of a light brown powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05856474
출처 데이터셋uspto-grants-1999_01
ORD IDord-65be74b59f924385abf637bd0ca4da83
출처 메모uspto-grants-1999_01