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HRID 27969作成日:2026年10月25日

Formate → Sodium 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylate

https://huagongshe.com/reaction/27969

反応式

関与物質

役割名称HCID仕込み量
反応物FormateHCID 283—
反応物Sodium AcetateHCID 517045—
反応物3-Acetoxymethyl 7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylic acidHCID 131711503—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物Sodium 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylateHCID 1317117360.95%

反応手順

10 g of the formate solvate of the syn isomer of 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylic acid (described in Belgium Pat. No. 850,662) were added at room temperature to a solution of 3.5 g of sodium acetate in 5 ml of water and 300 ml of ethanol and when dissolution was complete, the mixture was filtered. The filtrate was added dropwise over one hour with stirring at room temperature to 160 ml of absolute ethanol and the resulting mixture was stirred at room temperature for 3 hours and at 0° C. for 16 hours. The mixture was vacuum filtered and the crystals were washed with ethanol and dried under reduced pressure to obtain 7.75 g of the crystalline D form of the syn isomer of sodium 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylate containing 0.95% of water.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04224371
出典データセットuspto-grants-1980_09
ORD IDord-39112f5f0b064c6794dc4d0d27cfd8e6
出典メモuspto-grants-1980_09