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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Pyrrolo(2,3-b)pyridineHCID 9222—
ReactantSodium HydroxideHCID 14798—
CatalystHCID 178418390HCID 178418390—
SolventFormic AcidHCID 284—
SolventTriethylamineHCID 8471—
Product1H,2H,3H-pyrrolo(2,3-b)pyridineHCID 1001188922%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932272B2
Source datasetuspto-grants-2011_04
ORD IDord-a5e3104d3b0c4989b81d750a0ee29b87
Source noteuspto-grants-2011_04