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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372755Generated: October 27, 2026

Phosphorus oxychloride → 1-Methyl-1H-pyrrolo[2,3-b]pyridine-3-carboxaldehyde

https://huagongshe.com/reaction/1372755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium BicarbonateHCID 516892—
ReactantN-methyl-7-azaindoleHCID 583068—
SolventDimethylformamideHCID 6228—
Product1-Methyl-1H-pyrrolo[2,3-b]pyridine-3-carboxaldehydeHCID 1044196083%

Reaction Conditions

Temperature0 °C

Reaction Steps

Phosphoryl chloride (5.15 ml, 55.3 mmol) was added dropwise to DMF (70 ml) under stirring at 0° C. After the reaction mixture was stirred at 0° C. for 10 minutes, a solution of 1-methyl-1H-pyrrolo(2,3-b)pyridine (4.87 g, 36.8 mmol) in DMF (5 ml) was added dropwise at the same temperature. After completion of the dropwise addition, the reaction mixture was stirred at 0° C. for 4 hours and at 60° C. for 3.5 hours. The reaction mixture was poured in ice water—a saturated aqueous solution of sodium bicarbonate to neutralize the mixture therewith, followed by extraction with chloroform. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from ethyl acetate eluate fractions, 1-methyl-1H-pyrrolo(2,3-b)pyridine-3-carbaldehyde (4.87 g, 83%) was obtained as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157487B2
Source datasetuspto-grants-2007_01
ORD IDord-e7656052d4f74f818c521ed9f1139b9e
Source noteuspto-grants-2007_01