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| 化学名: | オキサシリンナトリウム一水和物 | | 英語化学名: | Oxacillin sodium monohydrate | | 别名: | OXACILLIN NA;OXACILLIN SODIUM SALT HYDRATE VETRANAL,;4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylicacid, 3,3-diMethyl-6-[[(5-Methyl-3-phenyl-4-isoxazolyl)carbonyl]aMino]-7-oxo-,sodiuM salt, hydrate (1:1:1), (2S,5R,6R)-;Oxacillin sod;Oxacillin Sodium Salt ;(2S,5R,6R)-3,3-dimethyl-6-[[(5-methyl-3-phenyl-4-isoxazolyl)carbonyl]amino]-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, sodium salt, hydrate (1:1:1);5-Methyl-3-phenyl-4-isoxazol penicillin sodium monohydrate;Oxacillin sodium monohydrate | | CAS番号: | 7240-38-2 | | 分子式: | C19H20N3NaO6S | | 分子量: | 441.43 | | EINECS: | 629-150-0 | | カテゴリ情報: | Antibiotics for Research and Experimental Use;beta-Lactams (Antibiotics for Research and Experimental Use);Biochemistry;Stains and Dyes;Stains&Dyes, A to;beta-Lactam StructureEPA;1694 Pharmaceuticals&Personal Care Products;Alphabetic;Antibiotics;BactericidalAntibiotics;Chemical Structure;NeatsAnalytical Standards;O;Principle;Peptide Synthesis/Antibiotics;Inhibitors | | Mol File: | 7240-38-2.mol |  |
| 融点 | 188 C | | 沸点 | 687℃ | | 比旋光度 | D20 +201° (c = 1 in water) | | 屈折率 | 205 ° (C=1, H2O) | | 闪点 | >110°(230°F) | | 貯蔵温度 | Inert atmosphere,2-8°C | | 溶解性 | Freely soluble in water, soluble in methanol, practically insoluble in methylene chloride. | | 色 | White to Almost white | | PH | pH (30g/l, 25℃) : 4.5～7.5 | | 水溶解度 | Freely soluble in water | | Merck | 14,6904 | | BRN | 4287093 | | CAS データベース | 7240-38-2(CAS DataBase Reference) |
| | オキサシリンナトリウム一水和物 Usage And Synthesis |
| 外観 | 白色～ほとんど白色, 結晶～粉末又は塊 | | 溶解性 | 水に溶け、エタノール及びアセトンにほとんど溶けない。 | | 用途 | オキサシリンナトリウムHPLC定量用標準品。 | | 用途 | ペニシリン系抗生物質です。
ペニシリン結合タンパクに結合し、細胞壁の
合成阻害を示します。ブドウ球菌にも有効と
されています。 | | 用途 | ペニシリン系抗生物質です。
ペニシリン結合タンパク質に結合し、細胞壁
の合成阻害作用を示します。ブドウ球菌にも
有効とされています。 | | 効能 | 抗生物質, 細胞壁合成阻害薬 | | 説明 | Oxacillin was synthesized by Bristol-Myers Laboratories in 1961 starting with 6-aminopenicillanic acid. It was the first orally active and penicillinase-stable semisynthetic penicillin to be introduced clinically. Oxacillin is slightly less stable against gastric acid and shows a lower serum concentration than phenoxymethylpenicillin, but it is highly active against phenoxymethylpenicillinresistant Staphylococcus aureus. Oxacillin has been used by oral and intramuscular administration for therapy of respiratory tract, urinary tract, gynecological, and other infections caused by benzylpenicillin-resistant bacteria. | | 化学的特性 | White or almost white powder. | | Originator | Resistopen,Squibb,US,1962 | | 使用 | Semi-synthetic antibiotic related to Penicillin. Antibacterial. Dyes and metabolites. | | 使用 | Penicillin antibacterial. | | 定義 | ChEBI: Oxacillin sodium monohydrate is a hydrate. It contains an oxacillin sodium. | | Manufacturing Process | (A) Benzaldoxime: (Reference, Vogel, Textbook of Practical Organic Chemistry, page 883) -Materials: (Theoretical yield, 121.1 grams of free oxime), 106.1 grams (1.0 mol) of benzaldehyde (NF grade), 69.5 grams (1.0 mol) of hydroxylamine hydrochloride (practical grade), 68.0 grams (1.7 mol) of sodium hydroxide (pellet).
Procedure: The sodium hydroxide is dissolved in 200 ml water and the benzaldehyde is added. With continued stirring the hydroxylamine hydrochloride is added in portions. Some heat is developed and eventually the benzaldehyde dissolves. The solution is stirred for 15 minutes and then cooled in an ice-bath. A waxy, crystalline mass separates, and after further cooling it is collected by suction and dried in air. Yield is 86 to 149 grams. This crude material is suitable for step (B).
(B) Benzohydroximic Chloride: [Reference, G.W. Perrold et al, J. Am. Chem. Soc., 79, 462 (1957)] - Materials: 121 grams (0.77 mol) of crude benzaldoxime from step (A), 500 ml of 8.3 N hydrochloric acid, chlorine.
Procedure: The crude product from (A) is suspended in the hydrochloric acid, cooled in an ice-salt mixture, and chlorine is passed into the mixture with stirring for ? to 1 hour. Transient blue and green colors may be noticed in the mixture during this time. The temperature will probably rise to 3° to 5°C. The solid is collected by suction filtration and dried for an hour or so on the filter before use in (C). If at all possible, it should be used on the day of preparation. Yield is 71 grams (after 1? hours on the filter).
(C) 5-Methyl-3-Phenyl-4-Isoxazolecarboxylic Acid: [Reference, A. Quilico and R. Rusco, Gazz. Chim. Ital. 67, 589 (1937); C.A. 32, 21177] - Materials: 71 grams (0.45 mol) of crude benzohydroximic chloride from (E), 78 grams (0.60 mol) of ethyl acetoacetate (practical grade), 34 grams (0.60 mol) of sodium methoxide (95% minimum), 400 ml of methanol (reagent grade).
Procedure: The sodium methoxide is cautiously added in portions to 200 ml of methanol with stirring. Some heat is evolved. To this warm solution is rapidly added the ethyl acetoacetate with continued stirring. The solution is stirred for 10 minutes and then cooled in an ice-salt-acetone mixture (-25°C). If desired a Dry Ice-acetone cooling bath may be used to shorten the addition time. The crude material from (B) is dissolved in 200 ml of methanol. At this point it is probably easier to filter this mixture by suction to remove a large amount of insoluble solid, which is probably sodium chloride. The solid may be rinsed with more methanol.
The filtrate is chilled in ice-water and added to the cooled methanolic solution of the sodium derivative of ethyl acetoacetate at a rate which keeps the temperature of the re. action mixture below 0°C. The addition time will be 15 to 20 minutes if ice-salt-acetone is used as a coolant. This reaction is extremely exothermic.
The reaction mixture is stirred overnight at room temperature and filtered to remove the sodium chloride. The filtrate is stripped in vacuo and the crude ester (literature reports MP 48°C) is dissolved in 150 ml of ethanol; 28 grams (0.70 mol of sodium hydroxide in 90 ml of water is added and the solution is refluxed for 2 hours. After removal of the ethanol in vacuo the residue is dissolved in water and extracted twice with ether. Dissolved ether is removed from the aqueous solution in vacuo and it is acidified to pH 2 with concentrated hydrochloric acid.
The crystalline crude acid is dried briefly and then recrystallized from acetonitrile to give 32 grams of white product; MP 193° to 194.5°C (literature reports 189° to 190°C). Concentration of the mother liquor gives an additional 5 grams of material having a MP of 192.5 to 194°C. The 37 grams of material represents an 18% overall yield from benzaldehyde.
(D) The acid is converted to the acid chloride by reaction with thionyl chloride.
(E) 5-Methyl-3-Phenyl-4-Isoxazolylpenicillin: A solution of 4.43 grams of 5methyl-3-phenylisoxazole-4-carbonyl chloride in 120 ml acetone was added
gradually to a stirred solution of 4.32 grams of 6-aminopenicillanic acid in 168 ml of 3% aqueous sodium bicarbonate and 50 ml acetone. When addition was complete the mixture was stirred at room temperature for 4 hours and then extracted with ether (2 x 200 ml), only the aqueous phase being retained. This aqueous solution was covered with 50 ml ether and adjusted to pH 2 by the addition of N hydrochloric acid. After separating the layers, the aqueous phase was extracted with two further 50 ml portions of ether. The combined ether solutions (which at this stage contained the free penicillin acid) were washed with water and then neutralized by shaking with 20 ml N sodium bicarbonate solution. The aqueous phase was separated, washed with ether, and evaporated at low temperature and pressure to leave the crude sodium salt of 5-methyl-3-phenyl-4-isoxazolylpenicillin as a white solid, which was finally dried in vacuo over phosphorus pentoxide and found to weigh 7.34 grams. | | brand name | Bactocill (GlaxoSmithKline); Prostaphlin (Apothecon). | | Therapeutic Function | Antibacterial | | 接触アレルゲン | Oxacillin is a semisynthetic penicillin of the group M.
It is closely related to cloxacillin. |
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