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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704516Generated: October 29, 2026

HCID 88412251, compound → HCID 131716761, compound

https://huagongshe.com/reaction/704516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 88412251HCID 88412251—
ReactantHCID 131716762HCID 131716762—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 131716761HCID 13171676165.9%

Reaction Steps

In 100 ml of methylene chloride was dissolved 11.8 g of pivaloyloxymethyl 7-amino-3-[(2-methoxymethyl-5-methyl-s-triazolo[1,5-a]pyrimidin-7-yl)thiomethyl]-3-cephem-4-carboxylate.hydrochloride, and 5.82 g of benzthiazolylthio 2-(2-amino-4-thiazolyl)-2-(Z)-methoxyiminoacetate was added to the solution and the mixture was stirred at room temperature for 2 hours. The reaction mixture was washed with 100 ml of a 5% sodium acetate aqueous solution and further washed with water, dried over anhydrous magnesium sulfate and the solvent was distilled off. 100 ml of isopropanol containing 1.5 ml of conc. hydrochloric acid was added to the residue, and the mixture was thoroughly stirred and further stirred by adding 150 ml of ether. Then, precipitates were collected by filtration, washed with water and dried to obtain powder. This was dissolved in 50 ml of ethanol and filtered and the filtrate was added dropwise into 300 ml of ether. Precipitates were collected by filtration, washed with ether and dried to obtain 7.91 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04987129
Source datasetuspto-grants-1991_01
ORD IDord-841048684d1f4b7b9006a773da7669a1
Source noteuspto-grants-1991_01