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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701134Generated: October 26, 2026

Diethyl Ether → 2-Methyl-7-[2-(2-aminothiazol-4-yl)glyoxylamido]-3-cephem-4-carboxylic acid hydrochloride

https://huagongshe.com/reaction/1701134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-Methyl-7-[2-(2-formylaminothiazol-4-yl)glyoxylamido]-3-cephem-4-carboxylic acidHCID 131711493—
ReactantHCID 178427249HCID 178427249—
SolventMethanolHCID 887—
Product2-Methyl-7-[2-(2-aminothiazol-4-yl)glyoxylamido]-3-cephem-4-carboxylic acid hydrochlorideHCID 131711722—

Reaction Steps

To a suspension of 2-methyl-7-[2-(2-formylaminothiazol-4-yl)glyoxylamido]-3-cephem-4-carboxylic acid, which can be represented as 2-methyl-7-[2-(2-formylimino-2,3-dihydrothiazol-4-yl)glyoxylamido]-3-cephem-4-carboxylic acid, (3.0 g.) in methanol (60 ml.) was added dropwise phosphorus oxychloride (2.55 L g.) under ice-cooling and stirring, and the mixture was stirred for 3.5 hours at the same temperature and then for 30 minutes at room temperature. After the reaction, the reaction mixture was poured into diethyl ether (400 ml.). The precipitates were collected by filtration, washed with diethyl ether and then dried to give 2-methyl-7-[2-(2-aminothiazol-4-yl)glyoxylamido]-3-cephem-4-carboxylic acid hydrochloride, which can be represented as 2-methyl-7-[2-(2-imino-2,3-dihydrothiazol-4-yl)glyoxylamido]-3-cephem-4-carboxylic acid hydrochloride (2.2 g.), mp >270° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04191762
Source datasetuspto-grants-1980_03
ORD IDord-7e16bc96b628492c823d476f15a52e08
Source noteuspto-grants-1980_03