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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1609672생성일: 2026년 10월 25일

Ethyl Acetate → HCID 178418679, 화합물

https://huagongshe.com/reaction/1609672

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Sodium 2-ethylhexanoateHCID 23672331—
반응물7beta-[2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-allyloxyiminoacetamido]-3-chloromethyl-3-cephem-4-carboxylate trifluoroacetateHCID 131718144—
반응물HCID 178418632HCID 178418632—
용매Dimethyl SulfoxideHCID 679—
생성물HCID 178418679HCID 17841867934.2%

반응 단계

To a suspension of 1-methyl-4-(4,5-dihydroxy-2-pyridylcarbonyl)piperazine (800 mg) in dimethyl sulfoxide (8 ml) was added sodium 2-ethylhexanoate (840 mg). The solution was added dropwise to a solution of 7β-[2-(5-amino-1,2,4-thiadiazol- 3-yl) -2-allyloxyiminoacetamido]-3-chloromethyl-3-cephem-4-carboxylate trifluoroacetate (syn isomer) (965 mg) in dimethyl sulfoxide (7 ml) at room temperature. After being stirred for 4 hours, the mixture was poured into ethyl acetate (200 ml) and the resulting precipitates were collected by filtration. The precipitates were dissolved in water and then adjusted to pH 3.0 with aqueous sodium bicarbonate. The resulting solution was subjected to column chromatography on Diaion HP-20 using 15% aqueous isopropyl alcohol as an eluent and the objective fraction was lyophilized to give 7β-[2-(5-amino-1,2,4-thiadiazol-3-yl)-2-allyloxyiminoacetamido]-3-[1-methyl-4-(4,5-dihydroxy-2-pyridylcarbonyl)-1-piperazinio]methyl-3-cephem-4-carboxylate (syn isomer) (380 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05401734
출처 데이터셋uspto-grants-1995_03
ORD IDord-5c12a75cadde4c6695a76e3a616911db
출처 메모uspto-grants-1995_03