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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27969Generated: October 26, 2026

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

https://huagongshe.com/reaction/27969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormateHCID 283—
ReactantSodium AcetateHCID 517045—
Reactant3-Acetoxymethyl 7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylic acidHCID 131711503—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductSodium 3-acetoxymethyl-7-[2-(2-amino-4-thiazolyl)-2-methoxyimino-acetamido]-ceph-3-eme-4-carboxylateHCID 1317117360.95%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04224371
Source datasetuspto-grants-1980_09
ORD IDord-39112f5f0b064c6794dc4d0d27cfd8e6
Source noteuspto-grants-1980_09