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HRID 542911作成日:2026年10月27日

Ceftazidime → (6R,7R)-7-[[(2E)-2-(2-Amino-1,3-thiazol-4-yl)-2-(2-carboxypropan-2-yloxyimino)acetyl]amino]-8-oxo-3-(pyridin-1-ium-1-ylmethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate;pentahydrate

https://huagongshe.com/reaction/542911

反応式

関与物質

役割名称HCID仕込み量
反応物CeftazidimeHCID 5481173—
溶媒Formic AcidHCID 284—
生成物(6R,7R)-7-[[(2E)-2-(2-Amino-1,3-thiazol-4-yl)-2-(2-carboxypropan-2-yloxyimino)acetyl]amino]-8-oxo-3-(pyridin-1-ium-1-ylmethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate;pentahydrateHCID 5362051—

反応条件

温度5 °C

反応手順

A second 128 ml aliquot of the ceftazidime solution prepared as described above was cooled and maintained at 5° C., while the pH was adjusted from 5.8 to 3.6 with 10.5 ml of 5.9M formic acid. The stirred solution was seeded with ceftazidime pentahydrate crystals and crystallization commenced. After 5 hours the crystals were harvested by filtration, washed with 150 ml of chilled water and 100 ml of chilled acetone and air dried to give 20.8 g of ceftazidime pentahydrate. The material assayed as follows: HPLC potency 84.4% (as is); polymer (stressed material) 0.66%; related substances, 1.07%; Karl Fischer 14.1%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04659813
出典データセットuspto-grants-1987_04
ORD IDord-0dabe3162f394c3c9bfcf7d27151ad10
出典メモuspto-grants-1987_04