Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | (4-Chloro-1-ethyl-1H-pyrazolo[3,4-b]pyridin-5-yl)methanol | HCID 20209064 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13732607 | HCID 13732607 | 67.5% |
Reaction Steps
Wet MnO2 (110 g) was refluxed for 90 minutes in 1 L of toluene with a Dean-stark trap for the separation of water. This suspension was then cooled and the 4-chloro-1-ethyl-1H-pyrazolo-[3,4-b]pyridine-5-methanol (17.5 g, 82.7 mmole) was added in 50 ml of toluene. The reaction mixture was then stirred for 6 hours and filtered with the aid of a filter pad. The toluene was evaporated and the residue added again to 100 g of wet MnO2 freshly prepared in the above manner. After additional 4 hours the reaction was briefly warmed at 55° and then filtered again through a filter pad. The residue which remained after evaporation of the toluene was purified by preparative high performance liquid chromatography (10% ethyl acetate/hexane, 250 ml/min) to yield 11.70 g of 4-chloro-1-ethyl-1H-pyrazolo[3,4-b]pyridine-5-carboxaldehyde, mp 89°-90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04622326 |
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| Source dataset | uspto-grants-1986_11 |
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| ORD ID | ord-b3c042ebecd448a68e2c6ec19ce593d7 |
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| Source note | uspto-grants-1986_11 |
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