Ammonia → 5-Benzyloxy-6-methyl-1H-indole-2-carboxylic acid methyl ester

HRID 881599Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 881599
[CH3:1][O:2][C:3](=[O:33])/[C:4](/OCC1C=CC=CC=1)=[C:5](/N=C=O)\[C:6]1[CH:11]=[C:10]([O:12][CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:9]([CH3:20])=[CH:8][C:7]=1Br.C([O-])(=O)C.[Cs+].[NH3:39]>CS(C)=O.[Cu]I>[CH3:1][O:2][C:3]([C:4]1[NH:39][C:7]2[C:6]([CH:5]=1)=[CH:11][C:10]([O:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[C:9]([CH3:20])[CH:8]=2)=[O:33]

Komponenten

6

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

To a solution of (Z)-3-(5-benzyloxy-2-bromo-4-methylphenyl)-2-benzyloxy-carbonylaminoacrylic acid methyl ester (0.2 g) and copper (I) iodide (0.075 g) in dimethylsulfoxide (8 mL) was added cesium acetate (0.38 g) at room temperature and this mixture was stirred under argon atmosphere at 90° C. for 5 hours. To this reaction mixture was added aqueous ammonia solution (28%) and the precipitated solid was collected by filtration, and washed with water, dried under reduced pressure to give the title compound (0.073 g).

Aufarbeitung

  1. filtrationthe precipitated solid was collected by filtration
  2. washwashed with water
  3. customdried under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-fa52f694ef9d47e1b91cc26d45b526b7
Quelldatensatz
uspto-grants-2015_03
Patentnummer
US08993616B2

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