HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704516Generated: October 29, 2026
HCID 88412251, compound → HCID 131716761, compound
https://huagongshe.com/reaction/704516
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 88412251 | HCID 88412251 | — |
| Reactant | HCID 131716762 | HCID 131716762 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131716761 | HCID 131716761 | 65.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04987129 |
|---|
| Source dataset | uspto-grants-1991_01 |
|---|
| ORD ID | ord-841048684d1f4b7b9006a773da7669a1 |
|---|
| Source note | uspto-grants-1991_01 |
|---|