N-(5-fluoro-2-oxo-2,3-dihydro-1H-indol-6-yl)-2-hydroxy-2-methyl-propionamide → N-{3-[5-(2-dimethylamino-ethyl)-3-methyl-4-oxo-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-2-ylmethylene]-5-fluoro-2-oxo-2,3-dihydro-1H-indol-6-yl}-2-hydroxy-2-methyl-propionamide

HRID 905872

Reaktionsgleichung

Reaktionsgleichung von HRID 905872
[CH3:1][N:2]([CH3:18])[CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][C:8]2[NH:11][C:12]([CH:15]=O)=[C:13]([CH3:14])[C:7]=2[C:6]1=[O:17].[F:19][C:20]1[CH:21]=[C:22]2[C:26](=[CH:27][C:28]=1[NH:29][C:30](=[O:35])[C:31]([OH:34])([CH3:33])[CH3:32])[NH:25][C:24](=[O:36])[CH2:23]2>>[CH3:1][N:2]([CH3:18])[CH2:3][CH2:4][N:5]1[CH2:10][CH2:9][C:8]2[NH:11][C:12]([CH:15]=[C:23]3[C:22]4[C:26](=[CH:27][C:28]([NH:29][C:30](=[O:35])[C:31]([OH:34])([CH3:32])[CH3:33])=[C:20]([F:19])[CH:21]=4)[NH:25][C:24]3=[O:36])=[C:13]([CH3:14])[C:7]=2[C:6]1=[O:17]

Komponenten

3

Versuchsvorschrift

The title compound was prepared under the same conditions as described in Example 112 with 5-(2-dimethylamino-ethyl)-3-methyl-4-oxo-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridine-2-carbaldehyde and N-(5-fluoro-2-oxo-2,3-dihydro-1H-indol-6-yl)-2-hydroxy-2-methyl-propionamide as starting materials to give N-{3-[5-(2-dimethylamino-ethyl)-3-methyl-4-oxo-4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridin-2-ylmethylene]-5-fluoro-2-oxo-2,3-dihydro-1H-indol-6-yl}-2-hydroxy-2-methyl-propionamide (40 mg, 41.8%) as a yellow solid.

Aufarbeitung

  1. customThe title compound was prepared under the same conditions

Quellen und Nachweise

ORD-Eintrag
ord-79e078ef88ea425381918c90577389ba
Quelldatensatz
uspto-grants-2011_09
Patentnummer
US08012966B2

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