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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731296Generated: October 26, 2026

4-Aminophenol → Ethyl 7-(4-Hydroxyanilino)-1H-pyrazolo[4,3-b]pyridine-6-carboxylate

https://huagongshe.com/reaction/1731296

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
ReactantSodium CarbonateHCID 10340—
ReactantEthyl 7-chloro-1H-pyrazolo[4,3-B]pyridine-6-carboxylateHCID 20038759—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductEthyl 7-(4-Hydroxyanilino)-1H-pyrazolo[4,3-b]pyridine-6-carboxylateHCID 13597392754.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04621089
Source datasetuspto-grants-1986_11
ORD IDord-bb145c7884934c8a9b9dac3e58acf3d0
Source noteuspto-grants-1986_11