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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-[2-(dimethylamino)ethoxy]benzaldehyde | HCID 10821605 | — |
| Reactant | 5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carboxamide | HCID 22449352 | — |
| Product | HCID 178437846 | HCID 178437846 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05958929 |
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| Source dataset | uspto-grants-1999_09 |
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| ORD ID | ord-49c77d89dd2542bcafb130749b2cda43 |
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| Source note | uspto-grants-1999_09 |
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