Potassium Carbonate → ethyl 3-(4-nitrophenyl)-1H-pyrrolo[3,2-b]pyridine-2-carboxylate

HRID 230546Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 230546
C(=O)([O-])[O-].[K+].[K+].Br[C:8]1[C:12]2=[N:13][CH:14]=[CH:15][CH:16]=[C:11]2[NH:10][C:9]=1[C:17]([O:19][CH2:20][CH3:21])=[O:18].[N+:22]([C:25]1[CH:30]=[CH:29][C:28](B(O)O)=[CH:27][CH:26]=1)([O-:24])=[O:23]>O1CCOCC1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[Pd]>[N+:22]([C:25]1[CH:30]=[CH:29][C:28]([C:8]2[C:12]3=[N:13][CH:14]=[CH:15][CH:16]=[C:11]3[NH:10][C:9]=2[C:17]([O:19][CH2:20][CH3:21])=[O:18])=[CH:27][CH:26]=1)([O-:24])=[O:23]

Komponenten

6

Versuchsvorschrift

3 g of potassium carbonate and 0.8 g of palladium tetrakis(triphenylphosphine) are added to a solution of 2 g of ethyl 3-bromo-1H-pyrrolo[3,2-b]pyridine-2-carboxylate and 1.5 g of 4-nitrophenylboronic acid in 50 ml of dioxane. The mixture is refluxed for 20 hours, and then filtered. The filtrate is concentrated under reduced pressure and the residue is purified by chromatography on a silica column, elution being carried out with a mixture of cyclohexane and ethyl acetate (50/50 by volume), to give 0.52 g of ethyl 3-(4-nitrophenyl)-1H-pyrrolo[3,2-b]pyridine-2-carboxylate, the characteristics of which are as follows:

Aufarbeitung

  1. temperatureThe mixture is refluxed for 20 hours
  2. filtrationfiltered
  3. concentrationThe filtrate is concentrated under reduced pressure
  4. customthe residue is purified by chromatography on a silica column, elution
  5. additionbeing carried out with a mixture of cyclohexane and ethyl acetate (50/50 by volume)

Quellen und Nachweise

ORD-Eintrag
ord-570c63974fce4ee6b9052ea3d84d19d1
Quelldatensatz
uspto-grants-2009_07
Patentnummer
US07566736B2

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