HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2080009Generated: November 2, 2026
1H-Pyrrolo(2,3-b)pyridine → 1H,2H,3H-pyrrolo(2,3-b)pyridine
https://huagongshe.com/reaction/2080009
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-Pyrrolo(2,3-b)pyridine | HCID 9222 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1H,2H,3H-pyrrolo(2,3-b)pyridine | HCID 10011889 | 22% |
Reaction Steps
1H-Pyrrolo[2,3-b]pyridine (1.00 g, 8.46 mmol) and 10% palladium-carbon (500 mg) were dissolved in a mixture of formic acid (10 mL) and triethylamine (10 mL), and the mixture was stirred at 70° C. for 87 hours. To this reaction mixture was further added 10% palladium-carbon (400 mg), and the solution was stirred for 9.5 hours at 70° C. The reaction mixture was cooled to room temperature, an aqueous solution of 5N sodium hydroxide was added thereto, the solution was extracted with ethyl acetate and tetrahydrofuran, and the organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated in vacuo, the residue was purified by silica gel column chromatography (ethyl acetate:methanol=10:1), and the title compound (219 mg, 1.82 mmol, 22%) was obtained as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07932272B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-a5e3104d3b0c4989b81d750a0ee29b87 |
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| Source note | uspto-grants-2011_04 |
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