| Identification | Back Directory | [Name]
PIVAMPICILLIN | [CAS]
33817-20-8 | [Synonyms]
mk191
PIVAPICILLIN
PIVAMPICILLIN
pivampiclillin
pivaloylampicillin
pivaloyloxymethylampicillinate
PIVAMPICILLIN EPP(CRM STANDARD)
ampicillinpivaloyloxymethylester
hydroxymethylester,pivalate(ester),d-(-)-do)-3-dimethyl-7-oxo-
4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylicacid,6-(2-amino-2-phenylacetami
6α-[[(R)-Aminophenylacetyl]amino]penicillanic acid (2,2-dimethyl-1-oxopropoxy)methyl ester
(2S,5R,6R)-6-(((2R)-Aminophenylacetyl)amino)3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid | [EINECS(EC#)]
251-688-6 | [Molecular Formula]
C22H29N3O6S | [MDL Number]
MFCD00869402 | [MOL File]
33817-20-8.mol | [Molecular Weight]
463.55 |
| Chemical Properties | Back Directory | [Appearance]
White or almost white, crystalline powder. | [Boiling point ]
679.0±55.0 °C(Predicted) | [density ]
1.33±0.1 g/cm3(Predicted) | [solubility ]
Practically insoluble in water, freely soluble in methanol, soluble in anhydrous ethanol. It dissolves in dilute acids. | [pka]
pKa 7.0 (Uncertain) | [Contact allergens]
Pivampicillin is a prodrug of ampicillin. It caused sensitization
in 56 workers at a penicillin factory. Pivampicillin
and pivmecillinam were responsible for contact dermatitis
in pharmaceutical production workers. Ampicillin,
mecillinam or amdinocillin, penicillin V and penicillin
G were also implicated in cross-reactions. |
| Hazard Information | Back Directory | [Description]
Pivampicillin caused sensitization in 56 workers at a
penicillin factory. Pivampicillin and pivmecillinam
were responsible for contact dermatitis in pharmaceutical
production workers. Ampicillin, mecillinam,
penicillin V and penicillin G were also implicated in
cross reactions. | [Chemical Properties]
White or almost white, crystalline powder. | [Originator]
Maxifen ,Sharp and Dohme, W. Germany ,1972 | [Uses]
Antibacterial. | [Definition]
ChEBI: Pivampicillin is a penicillanic acid ester that is the pivaloyloxymethyl ester of ampicillin. It is a prodrug of ampicillin. It has a role as a prodrug. It is a penicillanic acid ester and a pivaloyloxymethyl ester. It is functionally related to an ampicillin. | [Manufacturing Process]
(A) Pivaloyloxymethyl D(-)-α-azidobenzylpenicillinate: To a suspension of potassium D(-)α-azidobenzylpenicillinate (4.14 g) and potassium dicarbonate(1.5 g) in acetone (100 ml) and 10% aqueous sodium iodide (2 ml), chloromethyl pivalate (2.7 ml) was added and the mixture refluxed for 2 hours. After cooling, the suspension was filtered and the filtrate evaporated to dryness in vacuo. The remaining residue was washed repeatedly by decantation with petroleum ether to remove unreacted chloromethyl pivalate. The oily residue was taken up in ethyl acetate (100 ml), and the resulting solution washed with aqueous sodium bicarbonate and water, dried and evaporated in vacuo to yield the desired compound as a yellowish gum, which crystallized from ether, melting point 114°C to 115°C.
(B) Pivaloyloxymethyl D(-)-α-aminobenzylpenicillinate, hydrochloride: To a solution of pivaloyloxymethyl D(-)-α-azidobenzylpenicillinate (prepared as described above) in ethyl acetate (75 ml) a 0.2 M phosphate buffer (pH 2.2) (75 ml) and 10% palladium on carbon catalyst (4 g) were added, and the mixture was shaken in a hydrogen atmosphere for 2 hours at room temperature. The catalyst was filtered off, washed with ethyl acetate (25 ml) and phosphate buffer (25 ml), and the phases of the filtrate were separated. The aqueous phase was washed with ether, neutralized (pH 6.5 to 7.0) with aqueous sodium bicarbonate, and extracted with ethyl acetate (2 x 75 ml). To the combined extracts, water (75 ml) was added, and the pH adjusted to 2.5 with 1 N hydrochloric acid. The aqueous layer was separated, the organic phase extracted with water (25 ml), and the combined extracts were washed with ether, and freeze-dried. The desired compound was obtained as a colorless, amorphous powder.
The purity of the compound was determined iodometrically to be 91%. A crystalline hydrochloride was obtained from isopropanol with a melting point of 155°C to 156°C (dec.). | [Therapeutic Function]
Antibacterial |
|
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