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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276818Generated: October 31, 2026

1-(2-Aminoethyl)-4-(2-methoxyphenyl)piperazine → 3,4,5,7-Tetrahydro-6-carbethoxy-3-[2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl]pyrrolo[3',4':4,5]thieno[2,3-d]pyrimidin-4-one

https://huagongshe.com/reaction/276818

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Aminoethyl)-4-(2-methoxyphenyl)piperazineHCID 10399186—
Reactant2-Ethoxymethyleneamino-3,5-dicarbethoxy-4,6-dihydrothieno[3,2-c]pyrroleHCID 54410789—
SolventEthanolHCID 702—
Product3,4,5,7-Tetrahydro-6-carbethoxy-3-[2-(4-(2-methoxyphenyl)-1-piperazinyl)ethyl]pyrrolo[3',4':4,5]thieno[2,3-d]pyrimidin-4-oneHCID 1540712648.7%

Reaction Steps

1.1 g (4.8 mM) of 1-(2-aminoethyl)-4-(2-methoxyphenyl)-piperazine were added to 1.6 g (4.8 mM) of 2-ethoxymethyleneamino-3,5-dicarbethoxy-4,6-dihydrothieno[3,2-c]pyrrole in 25 ml of ethanol and refluxed for 2 h. The mixture was then concentrated in a rotary evaporator, and the crude product was purified by column chromatography (silica gel, mobile phase methylene chloride/methanol 96/4). After recrystallization from ethyl acetate, 1.1 g (47%) of product were isolated with melting point 153-155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355647B1
Source datasetuspto-grants-2002_03
ORD IDord-4448ccf54300443883f8be758cfa0479
Source noteuspto-grants-2002_03