戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 5528作成日:2026年10月23日

Ethyl Acetate → HCID 178418679、化合物

https://huagongshe.com/ja/reaction/5528

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Sodium 2-ethylhexanoateHCID 23672331—
反応物7beta-[2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-allyloxyiminoacetamido]-3-chloromethyl-3-cephem-4-carboxylate trifluoroacetateHCID 131718144—
反応物HCID 178418632HCID 178418632—
溶媒Dimethyl SulfoxideHCID 679—
生成物HCID 178418679HCID 17841867934.2%

反応手順

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 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05244890
出典データセットuspto-grants-1993_09
ORD IDord-1f2f42fc73044a5984d82eb3c72b03d5
出典メモuspto-grants-1993_09