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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 26323생성일: 2026년 10월 23일

Chloromethyl pivalate → 3-[(Acetyloxy)methyl]-7-[[2-carboethoxy-2-(1-pyrryl)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid pivaloyloxymethyl ester

https://huagongshe.com/ko/reaction/26323

반응식

참여 물질

역할이름HCID투입량
반응물Chloromethyl pivalateHCID 87885—
반응물SodiumHCID 5360545—
반응물3-[(Acetyloxy)methyl]-7-[[2-carboethoxy-2-(1-pyrryl)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]-oct-2-ene-2-carboxylic acidHCID 70605038—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물3-[(Acetyloxy)methyl]-7-[[2-carboethoxy-2-(1-pyrryl)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid pivaloyloxymethyl esterHCID 70606335—

반응 단계

The sodium salt of 3-[(acetyloxy)methyl]-7-[[2-carboethoxy-2-(1-pyrryl)acetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (3 grams) was added to about 40 ml of dry dimethylformamide (DMF) and stirred for about 30 minutes. Then 4.0 ml of chloromethyl pivalate in 5 ml of DMF was added. The mixture was stirred for about 4 hours at room temperature. This mixture is diluted with ethyl acetate and thoroughly washed with water. The ethyl acetate portion is dried over sodium sulfate, filtered and evaporated to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04148998
출처 데이터셋uspto-grants-1979_04
ORD IDord-49c37863b813497b83c0e60b15465c02
출처 메모uspto-grants-1979_04