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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894809Generated: October 30, 2026

Hydrochloric Acid → 7-[2-(2-Aminothiazol-4-yl)-2-(4-bromo-3-hydroxybenzyloxyimino)-acetamido]-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/894809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantHCID 131712351HCID 131712351—
SolventTetrahydrofuranHCID 8028—
Product7-[2-(2-Aminothiazol-4-yl)-2-(4-bromo-3-hydroxybenzyloxyimino)-acetamido]-3-cephem-4-carboxylic acidHCID 13171235284%

Reaction Steps

A mixture of 7-[2-(2-formamidothiazol-4-yl)-2-(4-bromo-3-hydroxybenzyloxyimino)acetamido]-3-cephem-4-carboxylic acid (syn isomer, 2.0 g.), conc. hydrochloric acid (1.1 g.), methanol (16 ml.) and tetrahydrofuran (10 ml.) was stirred at room temperature for 2 hours. After methanol was removed in vacuo, the residue was dissolved in a sodium bicarbonate aqueous solution and adjusted to pH 3.0 with 10% hydrochloric acid. The precipitates were collected by filtration, washed with water and dried over phosphorous pentoxide to give 7-[2-(2-aminothiazol-4-yl)-2-(4-bromo-3-hydroxybenzyloxyimino)-acetamido]-3-cephem-4-carboxylic acid (syn isomer, 1.6 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284631
Source datasetuspto-grants-1981_08
ORD IDord-e5ca3999e236429e8867b4806ef96b5b
Source noteuspto-grants-1981_08