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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675674Generated: October 31, 2026

Phosphorus oxychloride → Ethyl 4-chloro-1-ethyl-6-methyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylate

https://huagongshe.com/reaction/1675674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantPropanedioic acid, 2-(1-ethoxyethylidene)-, 1,3-diethyl esterHCID 99520—
Reactant1-Ethyl-1H-pyrazol-5-amineHCID 337310—
ProductEthyl 4-chloro-1-ethyl-6-methyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylateHCID 13059311—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 5-amino-1-ethylpyrazole (1.614 g, 14.5 mmol) and diethyl 2-(1-ethoxyethylidene)malonate [e.g. see J. Am. Chem. Soc., 1931, 53, 1836] (3.68 g) is heated at 150° C. under Dean Stark conditions for 5 hours. Phosphorous oxychloride (25 ml) is carefully added to the mixture and the resulting solution is heated at 130° C. under reflux for 18 hours. The mixture is concentrated in vacuo and the residual oil is carefully added, with cooling, to water (100 ml). The resulting mixture is extracted with dichloromethane (3×100 ml) and the combined organic extracts are dried over anhydrous sodium sulphate and concentrated in vacuo. The residual oil is purified by Biotage chromatography (silica; 90 g) eluting with 5% ethyl acetate in petroleum ether. Fractions containing the desired product are combined and concentrated in vacuo to give ethyl 4-chloro-1-ethyl-6-methyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003663B2
Source datasetuspto-grants-2011_08
ORD IDord-42a334e01d894c1d9bb5305c11175cbb
Source noteuspto-grants-2011_08