反応 #49825
ord-2598f6daf4df481c9a30d0b6858e1812
反応方程式
反応物
試薬
反応条件
後処理
- 1workup.STIRRINGunder stirring at room temperature for 4 hours
- 2ろ過The precipitate is filtered
- 3洗浄washed with acetonitrile
- 4濃縮The organic solution is concentrated in vacuo to a small volume
- 5workup.ADDITIONdiluted with water
- 6ろ過The obtained precipitate is filtered
- 7洗浄washed with water
- 8workup.DISSOLUTIONdissolved in chloroform
- 9洗浄washed with 1N HCl
- 10その他The organic solution is evaporated in vacuo to dryness
- 11その他the residue is purified over a SiO2 column
- 12その他Final crystallization from CH2Cl 2 /ethyl acetate
実験手順
Glycine methyl ester hydrochloride (0.7 g) suspended in anhydrous acetonitrile (250 ml) is treated with triethylamine (0.56 g) under stirring at room temperature. To the suspension first 3-(7-carboxy-1,4-dihydro-1-phenyl-indeno[1,2-c]pyrazole-3-yl)-2-cyano-3-oxo-N-phenyl-propanamide (2.3 g) and the dicyclohexylcarbodiimide (1.25 g) are added. The reaction mixture is kept under stirring at room temperature for 4 hours and then is basified to pH 8 by adding dimethylaminoethanol. The precipitate is filtered, washed with acetonitrile and then eliminated. The organic solution is concentrated in vacuo to a small volume, diluted with water, acidified to pH 2 with 1N HCl and then basified to pH 8 with 1N NaOH. The obtained precipitate is filtered, washed with water, dissolved in chloroform and washed with 1N HCl and then with water until neutral. The organic solution is evaporated in vacuo to dryness and the residue is purified over a SiO2 column using CHCl3 /methanol 90/10 as eluent. Final crystallization from CH2Cl 2 /ethyl acetate yields 1.2 g of pure N-[1,4-dihydro-1-phenyl-3-(2-phenylcarbamoyl-cyano-acetyl)indeno[1,2-c]pyrazol-7-yl] carbonyl-glycine methyl ester.