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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745421Generated: October 30, 2026

Hydrochloric Acid → 7-[2-(2-Aminothiazol-4-yl)-2-(2-methylthiazol-4-ylmethoxyimino)acetamido]-3-cephem-4-carboxylic acid hydrochloride

https://huagongshe.com/reaction/745421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant7-[2-(2-Formamidothiazol-4-yl)-2-(2-methylthiazol-4-yl methoxyimino)acetamido]-3-cephem-4-carboxylic acidHCID 131712338—
SolventMethanolHCID 887—
Product7-[2-(2-Aminothiazol-4-yl)-2-(2-methylthiazol-4-ylmethoxyimino)acetamido]-3-cephem-4-carboxylic acid hydrochlorideHCID 13171233996.7%

Reaction Steps

A mixture of 7-[2-(2-formamidothiazol-4-yl)-2-(2-methylthiazol-4-ylmethoxyimino)acetamido]-3-cephem-4-carboxylic acid (syn isomer, 240 mg.) and conc. hydrochloric acid (71 mg.) in methanol (2.5 ml.) was stirred at room temperature for 6.5 hours. After removing the solvent from the resultant solution in vacuo, the residue was triturated with diisopropyl ether. The precipitates were collected by filtration and washed with diisopropyl ether to give colorless crystals of 7-[2-(2-aminothiazol-4-yl)-2-(2-methylthiazol-4-ylmethoxyimino)acetamido]-3-cephem-4-carboxylic acid hydrochloride (syn isomer, 236 mg.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04598147
Source datasetuspto-grants-1986_07
ORD IDord-20bdd8c2597b475b945359460c2c252f
Source noteuspto-grants-1986_07