HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785584Generated: October 30, 2026
Hydrochloric Acid → 1H-Pyrrolo[2,3-b]pyridine-5-carboxylic acid
https://huagongshe.com/reaction/1785584
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1H-Pyrrolo(2,3-b)pyridine-5-carbonitrile | HCID 11788355 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 1H-Pyrrolo[2,3-b]pyridine-5-carboxylic acid | HCID 21907018 | — |
Reaction Steps
To a solution of 5-cyano-7-azaindole XXX (50 mg, 0.35 mmol) in ethanol (10 ml), 10% aqueous potassium hydroxide (15 ml) was added. The reaction was heated at 90° C. for two days after which the reaction was allowed to cool to room temperature. The pH was adjusted to 6 with 10% HCl and diluted with ethyl acetate (100 ml). The layers were separated and the aqueous layer was extracted with ethyl acetate (4×, 75 ml). The organic layers were combined and washed once with brine (100 ml) before drying over sodium sulfate. The organic layer was evaporated under reduced pressure to yield the titled product as an off-white solid. (52 mg, M−1, 161.2)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07504509B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-5ebf79b70122467190ee81021dc71ef2 |
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| Source note | uspto-grants-2009_03 |
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