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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065919Generated: November 2, 2026

Phosphorus oxychloride → HCID 131712733, compound

https://huagongshe.com/reaction/1065919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantAcetamide, 2-(trimethylsilyl)-HCID 357676—
Reactant3-Carbamoyloxymethyl-7-amino-3-cephem-4-carboxylic acidHCID 12784759—
Reactant2-(2-Aminothiazol-4-yl)-2-propargyloxyiminoacetic acidHCID 54372682—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
ProductHCID 131712733HCID 13171273385.9%

Reaction Steps

2-(2-Propynyl)oxyimino-2-(2-amino-1,3-thiazol-4-yl)acetic acid (syn isomer) (1.2 g) was suspended in tetrahydrofuran (15 ml). Phosphorus oxychloride (1.0 g) was added thereto at 0° to 5° C. and the mixture was stirred for 20 minutes at the same temperature. Trimethylsilylacetamide (0.5 g) was added thereto, the mixture was stirred for 20 minutes at the same temperature, phosphorus oxychloride (1.0 g) was added thereto, the resulting mixture was stirred for 20 minutes at 0° to 5° C., dimethylformamide (0.5 g) was added thereto and the resulting mixture was stirred for 1 hour at the same temperature. The resulting solution was added dropwise at -5° to 5° C. and pH 6.5 to 8.5 to a solution, which was prepared by adding acetone (10 ml) and tetrahydrofuran (10 ml) to a solution of 7-amino-3-carbamoyloxymethyl-3-cephem-4-carboxylic acid (1.9 g) in a mixture of sodium bicarbonate (0.4 g) and water (15 ml). The resulting mixture was stirred for 2 hours under ice-cooling keeping the pH of the mixture at 7.0 to 8.0 and then adjusted to pH 7.5. An insoluble material was filtered off and the filtrate was washed with ethyl acetate. The aqueous layer was adjusted to pH 6.0 and organic solvent in the aqueous layer was distilled off under reduced pressure. The remaining aqueous layer was adjusted to pH 4.0 and an insoluble material was filtered off. The filtrate was adjusted to pH 3.0 and precipitates were collected by filtration and dried to give 7-[2-(2-propynyl)oxyimino-2-(2-amino-1,3-thiazol-4-yl)acetamido]-3-carbamoyloxymethyl-3-cephem-4-carboxylic acid (syn isomer) (2.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04331664
Source datasetuspto-grants-1982_05
ORD IDord-4f2e87bba79b48c58d17c3b89a07c8b7
Source noteuspto-grants-1982_05