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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597848Generated: October 31, 2026

3-(2-Morpholin-4-ylethoxy)benzaldehyde → HCID 178437845, compound

https://huagongshe.com/reaction/1597848

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2-Morpholin-4-ylethoxy)benzaldehydeHCID 7164620—
Reactant5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carboxamideHCID 22449352—
ProductHCID 178437845HCID 178437845—

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 1-cyclopentyl-3-ethyl-5-amino-1H-pyrazole-4-carboxamide (1.05 g, 4.73 mmol), 3-[2-(4-morpholinyl)ethoxy]benzaldehyde (1.67 g) and xylenes (7 ml) was heated to 160° C. overnight. Additional aldehyde (0.4 g) was added and the mixture was heated at 160° C. until the reaction was complete. The reaction mixture was cooled to room temperature and a solid formed which was collected by filtration and washed with ether. The filtrate was concentrated to dryness and the residue was combined with the solid and was purified by column chromatography on silica gel eluting with ethyl acetate/ethanol (60/40). The solid product thus obtained was washed with ether, recrystallized from ethyl acetate and then washed with ether again to afford 1-cyclopentyl-3-ethyl-6-[3-[2-(4-morpholinyl)ethoxy]phenyl]-pyrazolo[3,4-d]pyrimidin-4-one, m.p. 173°-176° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736548
Source datasetuspto-grants-1998_04
ORD IDord-81e582e2746a4c73bac8e78647dda8ae
Source noteuspto-grants-1998_04