Pyrrolo [2,3-c] pyridine derivatives as p38 kinease inhibiting agents
a technology of pyridine derivatives and kineases, applied in the field of heterocyclic compounds, can solve the problems of adaptive hypertrophic response and decidedly negative consequences
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example 1
6-(1H-benzimidazol-2-ylmethyl)-3-(2,4,6-trifluorobenzoyl)-1,6-dihydro-7H-pyrrolo[2,3-c]pyridin-7-one
[0277]
Step A: N-(1H-benzimidazol-2-ylmethyl)-2,2-dimethoxyethanamine
[0278]
[0279]To a MeOH 150 mL suspension of 1-(1H-benzimidazol-2-yl)methanamine dihydrochloride (4.0 g, 18.2 mmol) were added dimethoxyacetaldehyde (1.89 g, 18.2 mmol, 60 wt. % solution in water), sodium acetate (7.45 g, 91 mmol) and sodium cyanoborohydride (9.09 mL, 9.09 mmol, 1.0 M THF solution). The reaction mixture was stirred at room temperature overnight, concentrated under reduced pressure and reconstituted in DCM (150 mL). The resulting suspension was filtered. The filtrate was concentrated and chromatographed on silica gel with a gradient solvent mixture (5% MeOH-DCM to 15% MeOH-DCM over 15 CV) to give the title compound as oil (3.1 g). LC / MS: m / z 205 (M+-OMe). 1H-NMR (CDCl3, 500 MHz) δ 3.02 (d, 1H), 3.36 (s, 6H), 4.40 (s, 2H), 4.52 (t, 1H), 7.28-7.32 (m, 2H), 7.58-7.62 (m, 2H), 8.78-8.92 (br.s, 1H).
Step B: N-...
example 2
[0285]6-[(4-fluoro-1H-benzimidazol-2-yl)methyl]-3-(2,4,6-trifluorobenzoyl)-1,6-dihydro-7H-pyrrolo[2,3-c]pyridin-7-one LC / MS: m / z 441 (M+H). 1H-NMR (500 MHz, d6-DMSO): δ: 5.50 (s, 2H), 6.99-7.03 (m, 2H), 7.15 (m, 1H), 7.32-7.37 (m, 3H), 7.59 (d, 1H), 7.91 (d, 1H), 13.09 (s, 1H).
example 3
[0286]6-[(4,5-difluoro-1H-benzimidazol-2-yl)methyl]-3-(2,4,6-trifluorobenzoyl)-1,6-dihydro-7H-pyrrolo[2,3-c]pyridin-7-one LC / MS: m / z 459 (M+H). 1H-NMR (500 MHz, d4-CD3OD:d6-DMSO=3:1): δ 5.62 (s, 2H), 7.21-7.28 (m, 3H), 7.31-7.37 (m, 1H), 7.41 (dd, 1H), 7.65 (d, 1H), 7.88 (s, 1H).
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