HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminophenol → Ethyl 7-(4-Hydroxyanilino)-1H-pyrazolo[4,3-b]pyridine-6-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Ethyl 7-chloro-1H-pyrazolo[4,3-B]pyridine-6-carboxylate | HCID 20038759 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 7-(4-Hydroxyanilino)-1H-pyrazolo[4,3-b]pyridine-6-carboxylate | HCID 135973927 | 54.5% |
Reaction Steps
Ethyl 7-chloro-1H pyrazolo[4,3-b]pyridine-6-carboxylate (1.0 g, 0.004 mole) and p-aminophenol (1.0 g, 0.009 mole) were stirred together in ethyl acetate (200 ml) under nitrogen for 48 hours, the temperature being maintained between -10° and -5° C. The ethyl acetate was removed under reduced pressure to give a yellow solid. This solid was dissolved in aqueous ethanol and the pH adjusted to pH8 with 10% sodium carbonate solution. The resulting solid was filtered off washed with water and dried. Recrystallization from methanol/ethyl acetate gave the title compound as a pale yellow solid (650 mg, 50%), m.p. 286°-287° C. (decomposition)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04621089 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-bb145c7884934c8a9b9dac3e58acf3d0 |
| Source note | uspto-grants-1986_11 |