HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 1-Ethyl-1H-pyrazolo[3,4-b]pyridine-4,5-dicarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Cyano-1-ethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid, ethyl ester | HCID 86757583 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Ethyl-1H-pyrazolo[3,4-b]pyridine-4,5-dicarboxylic acid | HCID 18354323 | 50% |
Reaction Steps
4-Cyano-1-ethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid, ethyl ester (2.0 g, 8.2 mmol) was suspended in ethanol (20 mL), and an aqueous solution of NaOH (6 N, 3 eq) was added. The reaction mixture was heated at reflux for 2 h and then diluted with water (100 mL). This aqueous solution was extracted with diethyl ether (50 mL×2) and the organic extracts were discarded. The aqueous layer was then acidified with phosphoric acid and extracted with EtOAc (50 mL×3). The extracts were concentrated via evaporation under reduced pressure to afford the title compound (>90% purity, 50-90% yield). This material was used directly without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06316438B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-1145d9fad09f4256a70f1d7f841bd58f |
| Source note | uspto-grants-2001_11 |