HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408558Generated: October 29, 2026
Sodium Bicarbonate → 2-Methyl-5-oxo-4-{3-[6-(propan-2-yloxy)pyridin-3-yl}-1H-indazol-5-yl]-1,4,5,7-tetrahydrofuro-[3,4-b]pyridine-3-carbonitrile
https://huagongshe.com/reaction/408558
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | [6-(Propan-2-yloxy)pyridin-3-yl]boronic acid | HCID 44754864 | — |
| Reactant | HCID 178428406 | HCID 178428406 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-Methyl-5-oxo-4-{3-[6-(propan-2-yloxy)pyridin-3-yl}-1H-indazol-5-yl]-1,4,5,7-tetrahydrofuro-[3,4-b]pyridine-3-carbonitrile | HCID 46911270 | 19.6% |
Reaction Steps
To a degassed solution of 120 mg (0.323 mmol) 4-(3-bromo-1H-indazol-5-yl)-2-methyl-5-oxo-1,4,5,7-tetrahydrofuro[3,4-b]pyridine-3-carbonitrile (Example 24) and 70.2 mg (0.388 mmol) [6-(propan-2-yloxy)pyridin-3-yl]boronic acid in anhydrous 1,4-dioxane (3.5 ml) were added under inert gas atmosphere 37.4 mg (0.032 mmol) tetrakis(triphenylphosphine)palladium(0) and aqueous sodium bicarbonate solution (2 M, 0.77 ml). The resulting mixture was stirred at 100° C. for 12 h. After cooling to room temperature and concentration under reduced pressure, the remaining solid was dissolved in ethyl acetate (20 ml). The solution was subsequently washed with water and brine, dried over sodium sulfate and concentrated under reduced pressure. The crude product was purified by preparative RP-HPLC (acetonitrile/water gradient, final mixture 95:5 v/v) to yield the title compound as a white solid (27 mg, 19% of th.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759341B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-b9d2cb5b011247199a4fa4f996baa603 |
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| Source note | uspto-grants-2014_06 |
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