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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 619239Generated: October 30, 2026

Methanol → HCID 88199116, compound

https://huagongshe.com/reaction/619239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantAcetamide, N-(trimethylsilyl)-HCID 25989—
Reactant(6R,7R)-7-Amino-3-ethenyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 7280824—
ReactantHCID 22118566HCID 22118566—
SolventDichloromethaneHCID 6344—
ProductHCID 88199116HCID 881991167.2%

Reaction Steps

To a solution of 7β-amino-3-vinyl-3-cephem-4-carboxylic acid (1 g) and N-(trimethylsilyl)acetamide (5.8 g) in dichloromethane (10 ml) was added 2-(2-amino-5-chlorothiazol-4-yl)-2-(Z)-(acetoxyimino) acetyl chloride (1.69 g) under ice-cooling. After being stirred at the same temperature for 1 hour, to this mixture was added methanol (10 ml). After evaporating in vacuo to remove the dichloromethane, the residue was added conc. hydrochloric acid (1.95 ml) at room temperature. After being stirred at the same temperature for 4 hours, the mixture was poured into water (10 ml). The mixture was adjusted to pH 3.5 with 28% ammonium hydroxide in water, and the resulting precipitate was collected by filtration to afford 7β-[2-(2-amino-5-chlorothiazol-4-yl)-2-(Z)-(hydroxyimino)acetamido]-3-vinyl-3-cephem-4-carboxylic acid (137 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05958914
Source datasetuspto-grants-1999_09
ORD IDord-2c9848e7c51541a48c8465f4993b24b0
Source noteuspto-grants-1999_09