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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831475Generated: October 31, 2026

1-(6-Ethoxy-5-formyl-3-pyridylsulfonyl)-4-ethylpiperazine → 4-{6-ethoxy-5-[3-ethyl-4,5,6,7-tetrahydro-7-oxo-2-(2-pyridylmethyl)-2H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-pyridinylsulfonyl}-1-ethylpiperazine

https://huagongshe.com/reaction/1831475

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(6-Ethoxy-5-formyl-3-pyridylsulfonyl)-4-ethylpiperazineHCID 22052236—
Reactant4-amino-5-ethyl-1-(2-pyridylmethyl)-1H-pyrazole-3-carboxamideHCID 22052237—
SolventTolueneHCID 1140—
Product4-{6-ethoxy-5-[3-ethyl-4,5,6,7-tetrahydro-7-oxo-2-(2-pyridylmethyl)-2H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-pyridinylsulfonyl}-1-ethylpiperazineHCID 2205223352%

Reaction Steps

A solution of 1-(6-ethoxy-5-formyl-3-pyridylsulfonyl)-4-ethylpiperazine(1.1 g, 4.9 mmol, from step (a) above) and 4-amino-5-ethyl-1-(2-pyridylmethyl)-1H-pyrazole-3-carboxamide (1.2 g, 4.9 mmol) in toluene (10 mL) was heated to reflux for 4 hours and the solution was concentrated under vacuum. The resulting product was recrystallised from ethyl acetate to give a pale brown solid (1.4 g, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067660B2
Source datasetuspto-grants-2006_06
ORD IDord-806039f3b87c4aab968ec134fb833c16
Source noteuspto-grants-2006_06