HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65991Generated: October 30, 2026
Isoamyl Alcohol → HCID 70625226, compound
https://huagongshe.com/reaction/65991
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoamyl Alcohol | HCID 31260 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 22756855 | HCID 22756855 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 70625226 | HCID 70625226 | — |
Reaction Steps
To a solution of 1.61 g. of sodium (0.07 mol.) in 200 ml. of 3-methyl butanol, 17.1 g. of 4-chloro-2-methyl-6-phenyl-2H-pyrazolo[3,4-b]pyridine (0.07 mol.) are added and the mixture is refluxed for six hours while stirring. The cooled solution is agitated with water, the organic layer dried and then evaporated in vacuo to give 20 g. (97%) of oil. To 18.5 g. of the oil (0.063 mol.), dissolved in 50 ml. of ether, a solution of 14.6 g. of maleic acid (0.126 mol.) in 500 ml. of ether is added. The precipitated maleate of 2-methyl-4-(3-methylbutoxy)-6-phenyl-2H-pyrazolo [3,4-b]pyridine, at first oily, crystallizes on standing overnight, yield: 24.6 g. (83%); m.p. 114°-116°. Recrystallization from ethyl acetate gives a product which melts at 119°-120°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04129738 |
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| Source dataset | uspto-grants-1978_12 |
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| ORD ID | ord-69b56ea87f7d4a50a49798b3cbfd0d3d |
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| Source note | uspto-grants-1978_12 |
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