Réaction #49385

ord-5cb5ea9590ec49be94d9bad2c5ae3039

Équation de réaction

CC(C)(C)OC(=O)n1c(-c2ccc(N)c3c2C(=O)NC3=O)c(I)c2ccccc21
3-Amino-6-[1-(tert-butoxycarbonyl)-3-iodoindol-2-yl]phtalimide
C#CCCO
3-butyn-1-ol
O
water
CC(C)(C)OC(=O)n1c(-c2ccc(N)c3c2C(=O)NC3=O)c(C#CCCO)c2ccccc21
3-amino-6-[1-(tert-butoxycarbonyl)-3-(4-hydroxy-1-butynyl)indol-2-yl]phtalimide
Rendement 87.0%

Solvants

Conditions de réaction

Température
50°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Extractionextracted with ethyl acetate
  2. 2
    LavageThe organic layer was washed with saturated brine
  3. 3
    Séchagedried over anhydrous sodium sulfate
  4. 4
    AutreThe solvent was evaporated under reduced pressure
  5. 5
    Autrethe residue was purified by preparative thin-layer chromatography (chloroform/methanol=10/1)

Mode opératoire

3-Amino-6-[1-(tert-butoxycarbonyl)-3-iodoindol-2-yl]phtalimide (150 mg, 0.298 mmol) was dissolved in diethylamine (7.5 mL), and the solution was added with bis(triphenylphosphine)dichloropalladium (16.7 mg, 0.0234 mmol), copper iodide (11.4 mg, 0.0596 mmol) and 3-butyn-1-ol (0.226 mL, 2.98 mmol), followed by stirring at 50° C. for 3.7 hours under argon atmosphere. The reaction mixture was added with water and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by preparative thin-layer chromatography (chloroform/methanol=10/1) to obtain 3-amino-6-[1-(tert-butoxycarbonyl)-3-(4-hydroxy-1-butynyl)indol-2-yl]phtalimide (115 mg, yield 87%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07745641B2uspto-grants-2010_06