3-(Aminomethyl)-6-methyl-4-propylpyridin-2(1H)-oneacetate → N-((1,2-dihydro-6-methyl-2-oxo-4-propylpyridin-3-yl)methyl)-1-isopropyl-3-methyl-6-(1H-pyrrolo[2,3-b]pyridin-5-yl)-1H-indazole-4-carboxamide
Reaction equation
[CH:1]([N:4]1[C:12]2[CH:11]=[C:10]([C:13]3[CH:14]=[C:15]4[CH:21]=[CH:20][NH:19][C:16]4=[N:17][CH:18]=3)[CH:9]=[C:8]([C:22]([OH:24])=O)[C:7]=2[C:6]([CH3:25])=[N:5]1)([CH3:3])[CH3:2].[NH2:26][CH2:27][C:28]1[C:29](=[O:38])[NH:30][C:31]([CH3:37])=[CH:32][C:33]=1[CH2:34][CH2:35][CH3:36]>>[CH3:37][C:31]1[NH:30][C:29](=[O:38])[C:28]([CH2:27][NH:26][C:22]([C:8]2[C:7]3[C:6]([CH3:25])=[N:5][N:4]([CH:1]([CH3:3])[CH3:2])[C:12]=3[CH:11]=[C:10]([C:13]3[CH:14]=[C:15]4[CH:21]=[CH:20][NH:19][C:16]4=[N:17][CH:18]=3)[CH:9]=2)=[O:24])=[C:33]([CH2:34][CH2:35][CH3:36])[CH:32]=1Participants
Reactant 2
Product 1
Procedure
The title compound was prepared in the same manner as described for example 80 (step c) from 1-isopropyl-3-methyl-6-(1H-pyrrolo[2,3-b]pyridin-5-yl)-1H-indazole-4-carboxylic acid (50 mg, 0.149 mmol) and 3-(aminomethyl)-6-methyl-4-propylpyridin-2(1H)-one (26 mg, 0.149 mmol) wherein the contents were stirred at RT for 5 h. The crude product was washed with DCM, filtered, and dried to afford the title compound as an off-white solid. (48 mg, 64%). 1H NMR (DMSO-d6, 400 MHz): δ 0.930 (t, J=7.6 Hz, 3H), 1.468 (d, J=6.4 Hz, 6H), 1.544-1.601 (m, 2H), 2.123 (s, 3H), 2.452 (s, 3H), 2.501 (s, 2H), 4.394 (d, J=4 Hz, 2H), 5.060-5.093 (m, 1H), 5.902 (s, 1H), 6.526 (s, 1H), 7.420 (s, 1H), 7.528 (s, 1H), 7.996 (s, 1H), 8.348 (s, 1H), 8.445 (s, 1H), 8.656 (s, 1H), 11.490 (brs, 1H), 11.735 (brs, 1H). LCMS (ES+) m/z: 497.49
Workup
- customThe title compound was prepared in the same manner
- washThe crude product was washed with DCM
- filtrationfiltered
- customdried
Sources & evidence
- ORD record
- ord-d4829b252a1543aa96de4e3ab0d40a1a
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09018382B2
Reaction notes
Loading…