反応 #49825

ord-2598f6daf4df481c9a30d0b6858e1812

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.STIRRINGunder stirring at room temperature for 4 hours
  2. 2
    ろ過The precipitate is filtered
  3. 3
    洗浄washed with acetonitrile
  4. 4
    濃縮The organic solution is concentrated in vacuo to a small volume
  5. 5
    workup.ADDITIONdiluted with water
  6. 6
    ろ過The obtained precipitate is filtered
  7. 7
    洗浄washed with water
  8. 8
    workup.DISSOLUTIONdissolved in chloroform
  9. 9
    洗浄washed with 1N HCl
  10. 10
    その他The organic solution is evaporated in vacuo to dryness
  11. 11
    その他the residue is purified over a SiO2 column
  12. 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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05424308uspto-grants-1995_06