反応 #522166
ord-8fc6fd006a1a4d35baa1593a84a53999
反応方程式
反応物
反応条件
後処理
- 1その他was subjected to catalytic reduction under ordinary pressure at room temperature
- 2その他After removing insoluble substance
- 3ろ過by filtration
- 4濃縮the filtrate was concentrated in vacuo
- 5workup.ADDITIONWater and ethyl acetate were added to the residue
- 6その他The insoluble substance was removed by filtration
- 7その他the aqueous layer was separated
- 8workup.ADDITIONEthyl acetate was added to the solution
- 9抽出extracted with ethyl acetate
- 10抽出The ethyl acetate solution and extract
- 11洗浄washed with a saturated aqueous solution of sodium chloride
- 12乾燥dried over magnesium sulfate
- 13濃縮The solution was concentrated in vacuo
- 14その他the residue was triturated with diethyl ether
- 15ろ過collected by filtration
実験手順
A suspension of 4-nitrobenzyl 7-[2-(2-formamidothiazol-4-yl)-2-n-propoxyiminoacetamido]-3-chloro-3-cephem-4-carboxylate (syn isomer, 2.4 g.), 10% palladium carbon (1.0 g.), methanol (24 ml.), water (3.6 ml.) and tetrahydrofuran (48 ml.) was subjected to catalytic reduction under ordinary pressure at room temperature. After removing insoluble substance by filtration, the filtrate was concentrated in vacuo. Water and ethyl acetate were added to the residue, and adjusted to pH 8 with a saturated aqueous solution of sodium bicarbonate. The insoluble substance was removed by filtration, and the aqueous layer was separated. Ethyl acetate was added to the solution, adjusted to pH 2.0 with hydrochloric acid and extracted with ethyl acetate. The ethyl acetate solution and extract were combined together, washed with a saturated aqueous solution of sodium chloride and dried over magnesium sulfate. The solution was concentrated in vacuo, and the residue was triturated with diethyl ether and collected by filtration to give 7-[2-(2-formamidothiazol-4-yl)-2-n-propoxyiminoacetamido]-3-chloro-3-cephem-4-carboxylic acid (syn isomer, 1.6 g.).