HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphenyl Ether → 1-ethyl-4-hydroxy-3-methyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphenyl Ether | HCID 7583 | — |
| Reactant | [[(1-Ethyl-3-methyl-5-pyrazolyl)amino]methylene]malonic acid diethyl ester | HCID 11380881 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-ethyl-4-hydroxy-3-methyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid ethyl ester | HCID 178469581 | — |
Reaction Steps
14.8 g. of [[(1-Ethyl-3-methyl-5-pyrazolyl)amino]methylene]malonic acid diethyl ester (0.05 mol.) are dissolved in 50 g. of diphenyl ether. The reaction mixture is heated to 235°-250° (bath temperature) and allowed to react at this temperature for 1 to 2 hours, while the resulting ethanol is continuously distilled off. The last part of the alcohol is removed by means of a water aspirator. The diphenyl ether is separated by distillation with a fractionating column in vacuo. The 1-ethyl-4-hydroxy-3-methyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid ethyl ester is obtained at b.p. 0.1-0.5 125°-129°, yield 10.7 g. (86%), m.p. 91°-93°. The compound is recrystallized from ligroin (90°-100°), m.p. 93°-94°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03983128 |
| Source dataset | uspto-grants-1976_09 |
| ORD ID | ord-1d47f8def5774200ade95ea253196c54 |
| Source note | uspto-grants-1976_09 |