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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597867Generated: October 31, 2026

Acetic Acid → HCID 178437836, compound

https://huagongshe.com/reaction/1597867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHCID 410450HCID 410450—
ReactantSodiumHCID 5360545—
Reactant5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carboxamideHCID 22449352—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductHCID 178437836HCID 17843783665.9%

Reaction Steps

Sodium spheres (0.42 g) were dissolved in ethanol (20 ml) and then 1-cyclopentyl-3-ethyl-5-amino-1H-pyrazole-4-carboxamide (2.02 g, 9.10 mmol) was added, followed by ethyl 2-[3-(4-morpholinyl)propoxy]benzoate (5.33 g). The reaction mixture was refluxed for 3 days, then stirred at room temperature, and then the solvent was stripped. The residue was dissolved in water (250 ml), acidified to a pH of about 7 with acetic acid and extracted with CHCl3. The organic layers were washed with brine, dried over MgSO4 and stripped to afford an oil. The oil was taken up in ether, filtered and the filtrate was stripped and purified by column chromatography on silica eluting with EtOAc (100%) followed by EtOAc/MeOH (80/20) to afford 2.71 g of 1-cyclopentyl-3-ethyl-6-[2-[3-(4-morpholinyl)propoxy]phenyl]pyrazolo[3,4-d]pyrimidin-4-one, as a liquid [labelled as Example 26(b)]. The free base was treated with EtOH.HCl and 1.14 g of the hydrochloride salt (labelled as Example 26(c) was obtained, m.p. 220°-221° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736548
Source datasetuspto-grants-1998_04
ORD IDord-9f10cbee9a904da789ded2fe188b5d31
Source noteuspto-grants-1998_04