1,2-Dichloroethane → (E)-N-methyl-N-(2-methyl-1H-indol-3-ylmethyl)-3-(2-oxo-2,3-dihydro-1H-pyrrolo[2,3-b]pyridin-5-yl)acrylamide

HRID 18311Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 18311
Cl.[O:2]=[C:3]1[CH2:11][C:10]2[C:5](=C[CH:7]=[C:8](/[CH:12]=[CH:13]/[C:14]([OH:16])=O)[CH:9]=2)[NH:4]1.O.OC1C2N=N[NH:24]C=2C=CC=1.C(N(C(C)C)CC)(C)C.[CH3:37][C:38]1[NH:39][C:40]2[C:45]([C:46]=1[CH2:47][NH:48][CH3:49])=[CH:44][CH:43]=[CH:42][CH:41]=2.C(Cl)CCl>CN(C=O)C>[CH3:49][N:48]([CH2:47][C:46]1[C:45]2[C:40](=[CH:41][CH:42]=[CH:43][CH:44]=2)[NH:39][C:38]=1[CH3:37])[C:14](=[O:16])/[CH:13]=[CH:12]/[C:8]1[CH:9]=[C:10]2[CH2:11][C:3](=[O:2])[NH:4][C:5]2=[N:24][CH:7]=1

Komponenten

7

Versuchsvorschrift

To a solution of (E)-3-(2-oxo-2,3-dihydro-1H-indol-5-yl)acrylic acid hydrochloride salt (0.50 g, 2.1 mmole), hydroxybenzotriazole monohydrate (0.31 g, 2.3 mmole), diisopropylethylamine (0.80 mL, 4.6 mmole), and 2-methyl-3-(methylaminomethyl)indole (0.40 g, 2.3 mmole) in DMF (50 mL) at RT was added EDC (0.46, 2.3 mmole). After 12 hr the reaction solution was concentrated under vacuum and the residue was purified by flash chromatography on silica gel (9:1 CHCl3/CH3OH containing 5% NH4OH) to give the title compound (0.66 g, 88%) as a light yellow solid: MS (ES) m/e 361 (M+H)+.

Aufarbeitung

  1. concentrationAfter 12 hr the reaction solution was concentrated under vacuum
  2. customthe residue was purified by flash chromatography on silica gel (9:1 CHCl3/CH3OH containing 5% NH4OH)

Quellen und Nachweise

ORD-Eintrag
ord-a5bcb270cc6d420182681a528e5abea9
Quelldatensatz
uspto-grants-2010_06
Patentnummer
US07741339B2

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