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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 619168Generated: November 2, 2026

3-[2-(dimethylamino)ethoxy]benzaldehyde → HCID 178437846, compound

https://huagongshe.com/reaction/619168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[2-(dimethylamino)ethoxy]benzaldehydeHCID 10821605—
Reactant5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carboxamideHCID 22449352—
ProductHCID 178437846HCID 178437846—

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 1-cyclopentyl-3-ethyl-5-amino-1H-pyrazole-4-carboxamide (3.50 g, 15.74 mmol), 3-[2-(dimethylamino)ethoxy]benzaldehyde (3.95 g) and xylenes (10 ml) was heated at 160° C. overnight. The reaction mixture was cooled to room temperature, the solvent was stripped, and the residue was partitioned between chloroform and water. The layers were separated, and the aqueous layer was extracted with chloroform. The organic layers were combined, washed with brine, dried over MgSO4, filtered and stripped to afford, as an oil, 1-cyclopentyl-3-ethyl-6-[3-[2-(dimethylamino)ethoxy]phenyl]pyrazolo[3,4-d]pyrimidin-4-one labelled as [Example 23 (b)]. The free base was treated with ethanolic HCl to afford the product as the hydrochloride salt [labelled as Example 23 (c)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05958929
Source datasetuspto-grants-1999_09
ORD IDord-49c77d89dd2542bcafb130749b2cda43
Source noteuspto-grants-1999_09