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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702736Generated: October 29, 2026

Water → HCID 131712824, compound

https://huagongshe.com/reaction/1702736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant7-Aminodeacetoxycephalosporanic acidHCID 33498—
Reactant5-Methyl-3-phenylisoxazole-4-carbonyl chlorideHCID 85624—
ReactantSodium BicarbonateHCID 516892—
SolventAcetoneHCID 180—
ProductHCID 131712824HCID 13171282468,849.797%

Reaction Conditions

Temperature0 °C

Reaction Steps

7-Aminodesacetoxycephalosporanic acid (7-amino-3-methylceph-3-em-4-carboxylic acid; 21.4 g., 0.1 mmole) was dissolved in 800 ml. of water by the action of sodium bicarbonate (27.9 g., 0.33 mmole). The solution was diluted with 800 ml. of acetone, and cooled to 0° C. 5-Methyl-3-phenylisoxazole-4-carbonyl chloride (27.7 g., 0.33 mmole) was added and the reaction mixture stirred for 2 hours at 0° C., then held at refrigerator temperature for approximately 16 hours. The acetone was removed by evaporation in vacuo, the aqueous residue extracted several times with ethyl acetate. Layering the aqueous phase with ethyl acetate and adjusting down to 2.0 precipitated the desired product. Filtration with ethyl acetate wash gave 3-methyl-7-(5-methylphenylisoxazole-4-carboxamido)ceph-3-em-4-carboxylic acid [27.5 g., pnmr (TMS/DMSO-d6) delta: includes 2.0 (s, 3H); 2.4 (s, 3H); 3.4 (m, 2H); 7.2-7.8 (m, 5H)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04348264
Source datasetuspto-grants-1982_09
ORD IDord-a8a4f747693e4e7aaf9b2387329d8e76
Source noteuspto-grants-1982_09