反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
In 30 ml of DMF were dissolved 3.22 g of 2-(2-amino-1,3-thiazol-4-yl)-2-{1-[3-(3,4-dihydroxybenzoyl)carbazoyl]-1-methylethoxyimino}acetic acid.hydrochloride, 5.32 g of diphenylmethyl 7-amino-3-[(2,5-bis(hydroxymethyl)-s-triazolo[1,5-a]pyrimidin-7-yl)thiomethyl]-3-cephem-4-carboxylate obtained in Example 42 and 1.38 g of 1-hydroxybenzotriazole and ice-cooled. Then, 1.86 g of DCC was added thereto and the mixture was stirred for 15 minutes under ice-cooling, and further stirred at room temperature for one hour. After the reaction mixture was filtered, 15 ml of chloroform was added thereto and the mixture was added dropwise into 2 liters of ether, precipitates were collected by filtration, washed with ether and then dried. Powder obtained was purified through silica gel column chromatography to obtain powder. A mixed solution of 30 ml of trifluoroacetic acid and 8 ml of anisole was ice-cooled and the powder previously obtained was added thereto, and the mixture was stirred for 30 minutes and added dropwise into 400 ml of ether. Precipitates were collected by filtration, washed with ether and then dried to obtain powder. The powder was suspended in 200 ml of water and dissolved at pH 7 by adding a 5% sodium hydrogencarbonate solution. After the resulting solution was adsorbed to 200 ml of HP 20 column filled with water, it was washed with water. Subsequently, the mixture was eluted with a 50% methanol-water. After evaporation of methanol, the residue was freeze-dried to obtain 4.16 g of the title compound.
WORKUP
后处理
- temperaturecooled
- temperaturecooling
- stirringfurther stirred at room temperature for one hour
- filtrationAfter the reaction mixture was filtered
- addition15 ml of chloroform was added
- additionthe mixture was added dropwise into 2 liters of ether
- customprecipitates
- filtrationwere collected by filtration
- washwashed with ether
- customdried
- customPowder obtained
- customwas purified through silica gel column chromatography
- customto obtain powder
- temperaturecooled
- customthe powder previously obtained
- additionwas added
- stirringthe mixture was stirred for 30 minutes
- customPrecipitates
- filtrationwere collected by filtration
- washwashed with ether
- customdried
- customto obtain powder
- dissolutiondissolved at pH 7
- washwas washed with water
- washSubsequently, the mixture was eluted with a 50% methanol-water
- customAfter evaporation of methanol
- customthe residue was freeze-dried