反応 #696710

ord-0c4a6676a21a42ebb6bd30574e7f0d2b

反応方程式

N=C=N
carbodiimide
O=C1CCC(=O)N1O
N-hydroxysuccinimide
O=C(NC1CCCCC1)NC1CCCCC1
dicyclohexylurea
C(=NC1CCCCC1)=NC1CCCCC1
dicyclohexylcarbodiimide
NCCc1ccc(O)cc1
tyramine

反応条件

温度
70°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他prepared above
  2. 2
    その他This is reacted at 70° C. for 90 minutes
  3. 3
    温度The mixture is cooled to 0° C.
  4. 4
    その他is recovered

実験手順

Formation of the tyramide of compound 111, is as follows. N-hydroxysuccinimide (33 mg) is dissolved in the reaction mixture prepared above by heating to 70° C., then dicyclohexylcarbodiimide (61 mg) is added. This is reacted at 70° C. for 90 minutes, an additional amount (6 mg) of the carbodiimide is added and the reaction is continued for another 30 minutes. The mixture is cooled to 0° C. and the precipitated dicyclohexylurea is settled by centrifugation. The supernatant, containing 6-(-4'-N-hydroxysuccinimidyl carboxy phenyl)-3,8-bis bromoacetamidyl-5 -methylphenanthridinium chloride (IV) is recovered. A solution of tyramine [4-(2'-amino)ethylphenol] (1.0 g) in water (5 ml) is formed by bringing it to pH 7 by addition of concentrated HCl. This solution is added to the supernatant containing compound IV and reacted at room temperature for one hour. This mixture is then reduced to a red oil by evacuation at 60° C., and is then extracted with water to remove excess tyramine. Compound (VI) is then recrystalized from ethanol-acidified with HCl.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05998135uspto-grants-1999_12