Cefaclor Property

Boiling point:

713.4±60.0 °C(Predicted)

Density 

1.3575 (rough estimate)

refractive index 

1.6100 (estimate)

storage temp. 

under inert gas (nitrogen or Argon) at 2–8 °C

solubility 

1 M HCl: 50 mg/mL, clear to very faintly turbid, yellow

pka

pKa 1.5±0.2(H2O) (Uncertain)

form 

powder

color 

Crystal

Water Solubility 

10g/L(temperature not stated)

BRN 

8176092

BCS Class

3

InChI

InChI=1S/C15H14ClN3O4S/c16-8-6-24-14-10(13(21)19(14)11(8)15(22)23)18-12(20)9(17)7-4-2-1-3-5-7/h1-5,9-10,14H,6,17H2,(H,18,20)(H,22,23)/t9-,10-,14-/m1/s1

InChIKey

QYIYFLOTGYLRGG-GPCCPHFNSA-N

SMILES

N12[C@@]([H])([C@H](NC([C@H](N)C3=CC=CC=C3)=O)C1=O)SCC(Cl)=C2C(O)=O

CAS DataBase Reference

53994-73-3(CAS DataBase Reference)

Safety

Hazard Codes 

Xn,Xi

Risk Statements 

42/43

Safety Statements 

22-36/37-45

WGK Germany 

2

RTECS 

XI0363000

HS Code 

29349990

Toxicity

TDLo orl-cld: 131 mg/kg/7D-I:MSK,SKN CMAJAX 126,1032,82

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H317May cause an allergic skin reaction

H334May cause allergy or asthma symptoms or breathing difficulties if inhaled

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P284Wear respiratory protection.

P304+P340IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing.

P342+P311IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician.

Cefaclor Chemical Properties,Usage,Production

Brand Name(s) in US

Ceclor

Description

Cefaclor differs from cephalexin primarily in the bio-isosteric replacement of methyl by chlorine at C-3 and is quite acid stable, allowing oral administration. It also is quite stable to metabolism. It is less active against Gram-negative bacteria compared with the other second-generation cephalosporins but is more active against Gram-negative bacteria compared with the first-generation drugs.

Description

Cefaclor is a cephalosporin antibiotic that is active against S. pyogenes, S. pneumoniae, S. aureus, P. mirabilis, S. typhi, E. coli, and H. influenzae (MICs = 0.25, 0.25-2, 1-2, 1, 0.5, 1, and 2-4 μg/ml, respectively). It is protective against S. pyogenes, S. pneumoniae, S. aureus, P. mirabilis, S. typhi, E. coli, and H. influenzae infections in mice (ED₅₀s = 0.08-30.2 mg/kg). Formulations containing cefaclor have been used in the treatment of various bacterial infections.

Chemical Properties

white crystalline solid

Originator

Ceclor,Lilly,US,1979

Uses

Cefaclor is used to study urinary tract, intra-abdominal, and?Haemophilus influenzae?infections. It is used to study the mechanism of human renal organic anion and peptide transporters such as hOAT1, hPEPT1, and hPEPT2 and to study the effects of inhibition of penicillin-binding proteins on bacterial cell wall mucopeptide synthesis.

Uses

radioopaque agent

Uses

Cefaclor belongs to the family of antibiotics known as the cephalosporins (cefalosporins). The cephalosporins are broad-spectrum antibiotics that are used for the treatment of septicaemia, pneumonia, meningitis, biliary-tract infections, peritonitis, and

Definition

ChEBI: A cephalosporin bearing chloro and (R)-2-amino-2-phenylacetamido groups at positions 3 and 7, respectively, of the cephem skeleton.

Manufacturing Process

Preparation of 7-amino-3-chloro-3-cephem-4-carboxylic acid: To a solution of 750 mg (185 mmol) of p-nitrobenzyl 7amino-3-chloro-3cephem-4-carboxylate hydrochloride in 20 ml of tetrahydrofuran and 40 ml of methanol was added a suspension of 750 mg of prereduced 5% palladium on carbon catalyst in 20 ml of ethanol and the suspension was hydrogenated under 50 psi of hydrogen at room temperature for 45 minutes. The catalyst was filtered and washed with THF and water. The filtrate and catalyst washes were combined and evaporated to dryness, The residue was dissolved in a water-ethyl acetate mixture and the pH adjusted to pH 3. The insoluble product was filtered and triturated with acetone. The product was then dried to yield 115 mg of 7- amino-3-chloro-3-cephem-4-carboxylic acid.
Preparation of 7-(D-α-phenylglycylamido)-3-chloro-3-cephem-4-carboxylic acid: To a suspension of 280 mg (1.2 mmol) of 7-amino-3-chloro-3-cephem- 4-carboxylic acid in 14 ml of acetonitrile was added with stirring at room temperature 0.5 ml of N,O-bis-(trimethylsilyl)acetamide to form the soluble disilylmethyl derivative thereof. The solution was cooled to 0 C and was slowly added to a solution of the mixed anhydride formed by reacting 408 mg (1.5 mmol) of methyl-3-α-carboxybenzylaminocrotonate sodium salt with 161 mg (1.7 mmol) of methyl chloroformate in the presence to 2 drops of N,N-dimethylbenzyl amine in 7 ml of acetonitrile.
The mixture was stirred at ice bath temperature for 2 hours, 1 ml of methanol was added and the mixture was filtered to remove insoluble impurities. Two milliliters of water were added to the filtrate and the pH was adjusted momentarily to pH 1.5, to effect removal of the enamine block, and then to pH 4.5 with triethylamine. After stirring for an additional hour at ice bath temperature the reaction product, 7-(D-α-phenylglycylamido)-3-chloro-3- cephem-4-carboxylic acid (zwitterion) precipitated from the reaction mixture as a crystalline solid. The product was filtered, washed with acetonitrile and dried in vacuo to yield 200 mg.

brand name

Ceclor (Lilly); Raniclor (Ranbaxy).

Therapeutic Function

Antibiotic

Antimicrobial activity

It is less resistant than other group 2 cephalosporins to staphylococcal β-lactamase. It is active against N. gonorrhoeae and H. influenzae and against most enterobacteria, but it is susceptible to common enterobacterial β-lactamases. Pr. vulgaris and Providencia, Acinetobacter and Serratia spp. are resistant. B. fragilis and clostridia are resistant but other anaerobes are commonly susceptible.

Pharmacokinetics

Oral absorption: c. 90%
C_max 250 mg oral: c. 6–7 mg/L after 50 min
Plasma half-life: 0.5–1 h
Volume of distribution: 0.37 L
Plasma protein binding: 25%
Absorption
Food intake increases the time taken to reach peak plasma levels and reduces the peak by 25–50%. The actual amount absorbed is unaffected. In children receiving 15 mg/kg per day (maximum daily dose 1 g) the mean peak serum level was 16.8 mg/L at 0.5–1 h. There is no accumulation of the drug during repeated administration.
Distribution
In patients receiving 500 mg every 8 h for 10 days, concentrations were 0–1.7 (mean 0.5) mg/L in mucoid sputum and 0–2.8 (mean 1.0) mg/L in purulent sputum. In children with chronic serous otitis media receiving 15 mg/kg per day, the mean peak concentration in middle ear secretion was 3.8 mg/L within 30 min of the dose when the mean simultaneous serum concentration was 12.8 mg/L.
Metabolism and excretion No metabolites have been identified, but the drug probably chemically degrades in serum. About half of the dose is recovered from the urine in the first 6 h and 70% in 24 h. Probenecid prolongs the plasma levels but in renal insufficiency the plasma half-life is only moderately increased. In patients with creatinine clearance values of 5–15 mL/min the mean plasma elimination half-life rose to 2.3 h and the 24 h urinary excretion fell to less than 10%. In patients requiring intermittent hemodialysis and receiving 500 mg every 8 h for 10 days, the half-life rose to 2.9 h. Dialysis removed 34% of the dose

Clinical Use

Cefaclor (Ceclor) is an orally active semisyntheticcephalosporin that was introduced in the American market in1979. It differs structurally from cephalexin in that the 3-methyl group has been replaced by a chlorine atom. It issynthesized from the corresponding 3-methylenecepham sulfoxideester by ozonolysis, followed by halogenation of theresulting β-ketoester. The 3-methylenecepham sulfoxideesters are prepared by rearrangement of the corresponding 6-acylaminopenicillanic acid derivative. Cefaclor is moderatelystable in acid and achieves enough oral absorption to provideeffective plasma levels (equal to about two-thirds of thoseobtained with cephalexin). The compound is apparentlyunstable in solution, since about 50% of its antimicrobial activityis lost in 2 hours in serum at 37°C. The antibacterialspectrum of activity is similar to that of cephalexin, but it isclaimed to be more potent against some species sensitiveto both agents. Currently, the drug is recommended for thetreatment of non–life-threatening infections caused by H.influenzae, particularly strains resistant to ampicillin.

Clinical Use

Uses are similar to those of other group 2 cephalosporins. It is among the few suitable for use in respiratory infections because of its activity against H. influenzae.

Side effects

Apart from mild gastrointestinal disturbance, the drug is well tolerated. Transiently increased transaminase levels and symptomatic vaginal candidosis have been noted. Clusters of a serum sickness-like illness have been described in children.

Safety Profile

Moderately toxic by intraperitoneal route. Human systemic effects by ingestion: joints, dermatitis, increased body temperature. An experimental teratogen. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of Clí, SOx, an

Synthesis

Cefaclor, (6R,7R)-7-[(R)-2-amino-2-phenylacetamido]-3-chloro-8-oxo-5-thia- 1-azabicyclo[4.2.0]oct-2-en-2-carboxylic acid (32.1.2.48), is synthesized from the most accessible antibiotic of this series, cefalotin (32.1.2.1), in which the carboxyl group is protected by esterification by a reaction with 4-nitrobenzylbromide in triethylamine, giving the 4-nitrobenzyl ester of 7-(2-thienylacetamido)-cephalosporanic acid (32.1.2.40). Reacting this with potassium ethyl xantogenate replaces the acetoxy group in the third position of the cephalosporin system, giving the corresponding S-derivative (32.1.2.41). Upon reducing this compound using zinc in formic acid, the product is desulfurized, giving the 4-nitrobenzyl ester of 3-exo-methylen-7-(2-thienylacetamido)-cefem-4-carboxylic acid (32.1.2.42). The exomethylene group is oxidized by ozone and the resulting dicarbonyl derivative tautomerizes to the enol form (32.1.2.43) upon reaction with sulfur anhydride. Then, the hydroxyl group is replaced with a chlorine atom upon reaction with thionyl chloride, giving the 4-nitrobenzyl ester of 3-chloro-7-(2-thienylacetamido)-3-cefem-4-carboxylic acid (32.1.2.44). The resulting product undergoes deacylation upon reaction with a mixture of pyridine with phosphorous pentachloride in isobutanol, forming the hydrochloride of 4-nitrobenzyl ester of 7-amino-3-chloro-3-cefem-4-carboxylic acid (32.1.2.45). This is acylated with an N-protected derivative of phenylglycine, (N-tert-butoxycarbonyl)-D-|á-phenylglycine in the presence of N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline in tetrahydrofuran, giving the product (32.1.2.46). The tert-butoxycarbonyl protection in this molecule is removed by heating in acetonitrile in the presence of p-toluenesulfonic acid. Finally, upon hydrogen reduction using zinc and hydrochloric acid in dimethylformamide, the 4-nitrobenzyl protecting group is removed from the resulting tosylate (32.1.2.47) giving cefaclor (32.1.2.48).

Veterinary Drugs and Treatments

Cefaclor may potentially be useful when an oral cephalosporin is desired to treat infections that are susceptible to it but resistant to first generation cephalosporins such as cephalexin or cefadroxil. Little information is available with regard to its clinical use in small animals, however.

Drug interactions

Potentially hazardous interactions with other drugs
Anticoagulants: effects of coumarins may be enhanced.

Metabolism

Cefaclor is rapidly excreted by the kidneys; up to 85% of a dose appears unchanged in the urine within 8 hours, the greater part within 2 hours. Probenecid delays excretion