Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 60155627 | HCID 60155627 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 58345029 | HCID 58345029 | 84% |
Reaction Steps
Benzoic acid (0.85 g, 7.1 mmol) and CDI (1.14 g, 7.1 mmol) were dissolved in DMA (36 ml). The reaction mixture was stirred for 1 h. 3-(3-(4-(aminomethyl)phenyl)-6-(pyridin-3-yl)-3H-imidazo[4,5-b]pyridin-2-yl)pyridin-2-amine hydrochloride was dissolved in DMA (40 ml) and the solution of benzoic acid and CDI was added over 10 min at room temperature. The reaction was stirred for two hours at room temperature and quenched by addition of water. The product N-(4-(2-(2-aminopyridin-3-yl)-6-(pyridin-3-yl)-3H-imidazo[4,5-b]pyridin-3-yl)benzyl)benzamide precipitated and was isolated by filtration, washed with water and ether, yielding 2.9 g (5.9 mmol, 84%) of the desired product in 98% purity. 1H NMR (DMSO-d6) 400 MHz δ: 9.15 (t, J=5.6 Hz, 1H), 9.01-9.00 (m, 1H), 8.67-8.66 (m, 1H), 8.63-8.62 (m, 1H), 8.58-8.57 (m, 1H), 8.22-8.19 (m, 1H), 8.02-8.00 (m, 1H), 7.95-7.92 (m, 2H), 7.57-7.45 (m, 8H), 7.29-7.27 (m, 1H), 7.03 (s, br, 2H), 6.45-6.42 (m, 1H), 4.59-4.58 (m, 2H) MS 498.55, [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501770B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-e83006c2ab284bd29ecfe8c6995e4b93 |
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| Source note | uspto-grants-2013_08 |
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