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HRID 1395414作成日:2026年10月25日

Pyridine → HCID 178477371、化合物

https://huagongshe.com/reaction/1395414

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Phosphorus pentachlorideHCID 24819—
反応物alpha-t-Butyloxycarbonylamino-alpha-[2-(chloroacetamido)thiazol-4-yl)acetic acidHCID 12763201—
反応物HCID 178477368HCID 178477368—
溶媒DichloromethaneHCID 6344—
生成物HCID 178477371HCID 17847737162.2%

反応手順

To a suspension of 349 mg of α-t-butyloxycarbonylamino-α-[2-(chloroacetamido)thiazol-4-yl ]acetic acid in 5 ml of methylene chloride is added 249 mg of phosphorous pentachloride, and the mixture is stirred at room temperature. The mixture is added dropwise under stirring to the solution of 494 mg of 7β-amino-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid diphenylmethyl ester dissolved in 5 ml of methylene chloride, followed by the addition of 474 mg of pyridine. After that, the stirring is continued for further 1 hour at room temperature. The reaction solution is washed with 0.5 N hydrochloric acid and then with wafer, and dried. The oily product obtained by the distillation of the solvent is purified by a column chromatography packed with silica gel. The procedure gives 513 mg of 7β-{α-t-butyloxycarbonylamino-α-[2-(chloroacetamido)thiazol-4-yl)acetamido}-3-(1-methyl-1H-tetrazol-5-ylthiomethyl)-3-cephem-4-carboxylic acid diphenylmethyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04203899
出典データセットuspto-grants-1980_05
ORD IDord-0b23d48082a641f58ea9beaa148af868
出典メモuspto-grants-1980_05