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cefaloglycin

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cefaloglycin Basic information

Product Name:
cefaloglycin
Synonyms:
  • (6R,7R)-7-[(R)-2-Amino-2-phenylacetylamino]-3-(acetoxymethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
  • Cephaloglycin(anhydrous)
  • Kafocin
  • Kefglycin
  • Lilly-39435
  • (6R,7R)-3-(acetoxymethyl)-7-[[(2R)-2-amino-2-phenyl-acetyl]amino]-8-keto-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
  • (6R,7R)-3-(acetyloxymethyl)-7-[[(2R)-2-amino-2-phenylacetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
  • (6R,7R)-3-(acetyloxymethyl)-7-[[(2R)-2-azanyl-2-phenyl-ethanoyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
CAS:
3577-01-3
MF:
C18H19N3O6S
MW:
405.42
EINECS:
222-696-7
Mol File:
3577-01-3.mol
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cefaloglycin Chemical Properties

Melting point:
236.5°C (rough estimate)
Boiling point:
217.4°C (rough estimate)
Density 
1.3328 (rough estimate)
refractive index 
1.6390 (estimate)
storage temp. 
2-8°C
solubility 
Aqueous Acid (Slightly), Methanol (Slightly, Heated)
form 
Solid
pka
pKa 1.71(H2O t=25±2 I=0.1 ) (Uncertain);7.29(H2O t=25±2 I=0.1 ) (Uncertain)
color 
White to Pale Brown
Water Solubility 
10.5g/L(25 ºC)
Stability:
Hygroscopic, Moisture Sensitive, Temperature Sensitive
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Safety Information

Hazard Codes 
Xn
Risk Statements 
42/43
Safety Statements 
36
Hazardous Substances Data
3577-01-3(Hazardous Substances Data)
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cefaloglycin Usage And Synthesis

Originator

Kefglycin,Shionogi,Japan,1969

Uses

Cefaloglycin is a first-generation cephalosporin antibiotic.

Uses

Antibacterial.

Definition

ChEBI: A cephalosporin antibiotic containing at the 7beta-position of the cephem skeleton an (R)-amino(phenyl)acetamido group.

Manufacturing Process

dl-Phenylglycine is resolved in a conventional manner by reaction with cinchonine, fractional crystallization of the resulting diastereoisomers, and acidification to release the phenylglycine enantiomorphs. D-phenylglycine, thus prepared, is reacted with carbobenzoxy chloride in a conventional manner to produce N-carbobenzoxy-D-phenylglycine.
A 0.60 g portion of N-carbobenzoxy-D-phenylglycine is dissolved in 10 ml of dry tetrahydrofuran. The solution is cooled in an ice-salt bath, and to it is added 0.29 ml of triethylamine with stirring over a period of 10 minutes, followed by 0.29 ml of isobutyl chloroformate, after which stirring is continued for 10 minutes at -5°C. During this time, 0.57 g of 7-aminocephalosporanic acid and 0.29 ml of triethylamine are dissolved in 5 ml of tetrahydrofuran and 5 ml of water, and the solution is centrifuged to remove a dark sludge. The clarified solution is cooled in ice and slowly added to the reaction mixture, and stirring is continued in the ice bath for 0.5 hour, followed by one hour at room temperature.
The reaction product mixture is a homogenous solution having a pH of about 6. It is evaporated under vacuum to a semisolid residue. To the residue are added 35 ml of water and a few drops of triethylamine to raise the pH to 8. The aqueous solution obtained thereby is extracted successively with 50 ml and 35 ml portions of ethyl acetate, the pH being adjusted to 2 at each extraction with hydrochloric acid. The extracts are combined, filtered, dried over sodium sulfate, stripped of solvent, and evaporated under vacuum. The product is 7-(N-carbobenzoxy-D-α-aminophenylacetamido)cephalosporanic acid in the form of a yellow-white amorphous solid weighing 1.10 g.
Of this material 1.0 g is dissolved in 150 ml of warm 95% ethyl alcohol. To the solution is added 1.0 g of 5% palladium on carbon catalyst, and the mixture is hydrogenated at room temperature and atmospheric pressure by bubbling hydrogen into it for 3 hours with stirring. The hydrogenation product is filtered. The solid phase, comprising the catalyst and the desired product, is suspended in ethyl acetate and water and adjusted to pH 2 with hydrochloric acid. The suspension is filtered to remove the catalyst. The aqueous phase is separated from the filtrate, and is evaporated under vacuum to recover the desired product, 7-(D-α-aminophenylacetamido)cephalosporanicacid.

brand name

Kafocin (Lilly).

Therapeutic Function

Antibacterial

cefaloglycin Preparation Products And Raw materials

Preparation Products

cefaloglycin Supplier

Beijing HuaMeiHuLiBiological Chemical
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010-56205725
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waley188@sohu.com
Shanghai Han-Xiang Chemical Co., Ltd.
Tel
15971444841
Email
amber@biochempartner.com
BOC Sciences
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16314854226; +16314854226
Email
inquiry@bocsci.com
Shaanxi Dideu Medichem Co. Ltd
Tel
+86-029-89586680 +86-18192503167
Email
1026@dideu.com
Shaanxi Dideu Medichem Co. Ltd
Tel
+86-029-81138252 +86-18789408387
Email
1057@dideu.com
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cefaloglycin (3577-01-3)Related Product Information