| Identification | Back Directory | [Name]
pheneticillin | [CAS]
147-55-7 | [Synonyms]
Penorale
Synthepen
Alfacilin
Phenoxy PC
NSC 117548
Feneticillin
pheneticillin
Phenethecillin
Phenoxyethylpenicillin
pheneticillin USP/EP/BP
1-Phenoxyethylpenicillin
a-Phenoxyethylpenicillin
Phenethicillin solution,100ppm
Phenethicillin Solution, 600ppm
6α-[(1-Oxo-2-phenoxypropyl)amino]penicillanic acid
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-(2-phenoxypropionamido)- (7CI, 8CI)
(2S,5R,6R)-3,3-Dimethyl-7-oxo-6-[(2-phenoxypropionyl)amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(1-oxo-2-phenoxypropyl)amino]-, [2S-(2a,5a,6b)]-
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(1-oxo-2-phenoxypropyl)amino]-, (2S,5R,6R)- (9CI) | [EINECS(EC#)]
205-691-4 | [Molecular Formula]
C17H20N2O5S | [MDL Number]
MFCD00869396 | [MOL File]
147-55-7.mol | [Molecular Weight]
364.42 |
| Hazard Information | Back Directory | [Originator]
Syncillin, Bristol, US ,1959 | [Uses]
Phenethicillin is a penicillin antibiotic medication. | [Definition]
ChEBI: A penicillin in which the substituent at position 6 of the penam ring is a 2-phenoxypropanamido group. | [Manufacturing Process]
Triethylamine (1.5 ml) was added to a cold solution (10°C) of αphenoxypropionic acid (1.66 g, 0.01 mol) in 15 ml of pure dioxane, with stirring and cooling to 5°C to 10°C while isobutyl chloroformate (1.36 g, 0.01 mol) in 5 ml of dioxane was added dropwise. Then the mixture was stirred for ten minutes at 5°C to 8°C. A solution of 6-amino-penicillanic acid (2.16 g, 0.01 mol) in 15 ml of water and 2 ml of triethylamine was then added dropwise while the temperature was maintained below 10°C. The resulting mixture was stirred in the cold for 15 minutes then at room temperature for 30 minutes, diluted with 30 ml of cold water and extracted with ether which was discarded. The cold aqueous solution was then covered with 75 ml of ether and acidified to pH 2 with 5 N H2SO4. After shaking, the ether layer containing the product 6-(α-phenoxypropionamido)penicillanic acid, was dried for ten minutes over anhydrous sodium sulfate and filtered. Addition of 6 ml of dry n-butanol containing 0.373 g/ml of potassium 2-ethylhexanoate precipitated the potassium salt of the product as a colorless oil which crystallized on stirring and scratching and was collected, dried in vacuo and found to weigh 2.75 g, to melt at 217°C to 219°C. | [Brand name]
Chemipen
(Bristol-Myers Squibb); Syncillin (Bristol-Myers
Squibb) [Name previously used: Phenethicillin.]. | [Therapeutic Function]
Antibacterial |
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