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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257020Generated: November 3, 2026

Benzene → HCID 178437875, compound

https://huagongshe.com/reaction/2257020

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 2-pyrrol-1-ylacetateHCID 350610—
ReactantTrimethylaluminumHCID 16682925—
Reactant5-amino-1-cyclopentyl-3-ethyl-1H-pyrazole-4-carboxamideHCID 22449352—
ProductHCID 178437875HCID 178437875—

Reaction Steps

To a solution of 1-cyclopentyl-3-ethyl-5-amino-1H-pyrazole-4-carboxamide (1.0 g, 4.5 mmol) in benzene (10 ml) in an ice bath was added trimethylaluminum (4.9 ml, 2M in toluene). The reaction mixture was stirred at room temperature for 1 hour, then 1-(ethoxycarbonylmethyl)pyrrole (0.7 g) in benzene (25 ml) was added and the reaction mixture was refluxed overnight. The reaction mixture was cooled, 2N HCl was added and the mixture was extracted with CHCl3 (3×). The organic layer was separated, dried over MgSO4, and concentrated in vacuo. The residue was digested with ether and recrystallized from ether to afford 1-cyclopentyl-3-ethyl-6-(1-pyrrolylmethyl)-pyrazolo[3,4-d]pyrimidin-4-one, m.p. 170°-172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05656629
Source datasetuspto-grants-1997_08
ORD IDord-48d9cac0971a46da9d1e13ba4a5f91d0
Source noteuspto-grants-1997_08