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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1577583Generated: October 29, 2026

Phosphorus oxychloride → HCID 131712380, compound

https://huagongshe.com/reaction/1577583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantAcetamide, 2-(trimethylsilyl)-HCID 357676—
ReactantSodium BicarbonateHCID 516892—
Reactant7-Amino-3-(1-methyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylicacidHCID 13020813—
ReactantHCID 54002447HCID 54002447—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 131712380HCID 13171238034.2%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of phosphorus oxychloride (1.6 g.) and N,N-dimethylformamide (31 ml.) was warmed at 40° C. for 30 minutes followed by cooling to -10° C. To the mixture was added 2-[N-(3-pyridyl)carbamoylmethoxyimino]-2-(2-formamidothiazol-4-yl)acetic acid (syn isomer) (3.1 g.) followed by stirring for an hour at -10° to -7° C. On the other hand, a mixture of 7-amino-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid (3.2 g.) and trimethylsilylacetamide (7 g.) in methylene chloride (60 ml.) was stirred for 30 minutes at room temperature and then cooled to -15° C. To the mixture was added the above obtained dimethylformamide mixture followed by stirring for 1.5 hours at -15° to -10° C. To the reaction mixture were added ice-cold water and sodium bicarbonate. The aqueous layer (pH 7 to 8) was separated and washed with ethyl acetate and then thereto was added ethyl acetate. After the pH was adjusted to 3 to 4 with 10% hydrochloric acid, the precipitates were collected and then dissolved in an aqueous solution of sodium bicarbonate. The resulting mixture was treated with activated charcoal and the aqueous layer was separated and then adjusted to pH 3 to 4 with 10% hydrochloric acid. The precipitates were collected by filtration and dried to give the title compound (2.0 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04288435
Source datasetuspto-grants-1981_09
ORD IDord-62852499a68b4248b90b2aff23ada007
Source noteuspto-grants-1981_09