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Dicyclohexylcarbodiimide → Diisopropyl ether ethanol

HRID 1939891
ノート
印刷プレビュー

反応式

HRID 1939891 の反応式
[OH:1][C:2]1[C:10]2N=NNC=2C=C[CH:3]=1.[CH:11]1(N=C=NC2CCCCC2)[CH2:16]CCC[CH2:12]1>CN(C)C=O>[CH2:2]([OH:1])[CH3:3].[CH:11]([O:1][CH:2]([CH3:3])[CH3:10])([CH3:16])[CH3:12]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 10868DicyclohexylcarbodiimideHCID 178418300HCID 178418300、化合物

生成物 1

HCID 23358034Diisopropyl ether ethanol

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
5 °C

実験手順

Then, at 20° C., 18.3 g (0.12 mol) of hydroxybenzotriazole (HOBT), 23.7 g (0.109 mol) of N-4-trifluoromethylbenzyl-N-n-propylamine and 25.6 g (0.125 mol) of dicyclohexyl-carbodiimide (DCCI) and a further 250 ml of dimethylformamide (DMF) were added. The mixture was left to react for 24 hours. It was then cooled to 5° C. and filtered. 500 ml of water were added to the filtrate and it was extracted with ethyl acetate. The combined organic phases were washed with water and saturated sodium hydrogen carbonate solution, dried with magnesium sulphate and filtered over kieselguhr/char-coal. After working up in the usual way, 50 g of colourless crystals of the title compound are obtained by crystallisation from ethanol/diisopropylether (1:1). The 3H-PAF-receptor bonding--determined using human thrombocytes--is Ki =1.8 nMol/liter. (The method used is described for example in European Patent Application 368 175).

後処理

  1. waitThe mixture was left
  2. customto react for 24 hours
  3. filtrationfiltered
  4. addition500 ml of water were added to the filtrate and it
  5. extractionwas extracted with ethyl acetate
  6. washThe combined organic phases were washed with water and saturated sodium hydrogen carbonate solution
  7. dry with materialdried with magnesium sulphate
  8. filtrationfiltered over kieselguhr/char-coal

出典と根拠

ORDレコード
ord-ca2cdcfad3ee4f1285418e0b70278f44
出典データセット
uspto-grants-1997_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05698552

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート