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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596791Generated: October 30, 2026

Water → HCID 131710661, compound

https://huagongshe.com/reaction/596791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiketeneHCID 12661—
ReactantSodium BicarbonateHCID 516892—
Reactant7-Amino-3-(6-methyl-1-oxidopyridazin-3-yl)thiomethyl-3-cephem-4-carboxylic acidHCID 70634304—
SolventAcetoneHCID 180—
ProductHCID 131710661HCID 131710661—

Reaction Steps

A mixture of 0.354 g. of 7-amino-3-(6-methyl-1-oxidopyridazin-3-yl)thiomethyl-3-cephem-4-carboxylic acid, 0.42 g. of sodium hydrogen carbonate, 5 ml. of water and 5 ml. of acetone is cooled to 5° C and under stirring, 0.2 g. of diketene is added. The mixture is further stirred at room temperature for 30 minutes. The acetone is distilled off under reduced pressure and the residue is washed with ethyl acetate. The water layer is separated, brought to pH 2 with 50 % phosphoric acid, saturated with sodium chloride and extracted three times with ethyl acetate. The extracts are pooled, washed with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, concentrated and allowed to stand under cooling with ice. The resultant crystals are loosened with the addition of ether and recovered by suction-filtration. The procedure gives 7-acetoacetamido-3-(6-methyl-1-oxidopyridazin-3-yl) thiomethyl-3-cephem-4-carboxylic acid as crystals melting at 85°-87° C(decomp.). Yield 0.13 g. (30 %).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04012379
Source datasetuspto-grants-1977_03
ORD IDord-bb8acd012e9245d1b33858e8cd30c9b4
Source noteuspto-grants-1977_03