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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-methyl-7-azaindole | HCID 583068 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Methyl-1H-pyrrolo[2,3-b]pyridine-3-carboxaldehyde | HCID 10441960 | 83% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157487B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-e7656052d4f74f818c521ed9f1139b9e |
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| Source note | uspto-grants-2007_01 |
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