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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902477Generated: October 30, 2026

Furan → 4-[4-(Furan-2-carbonyl)-piperazin-1-yl]-6-oxo-6,7-dihydro-thieno[2,3-b]-pyridine-5-carbonitrile

https://huagongshe.com/reaction/902477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFuranHCID 8029—
Reactant1-(Furan-2-yl)piperazineHCID 19763577—
Reactant4-Chloro-6-oxo-6,7-dihydro-thieno[2,3-b]pyridine-5-carbonitrileHCID 59702118—
Product4-[4-(Furan-2-carbonyl)-piperazin-1-yl]-6-oxo-6,7-dihydro-thieno[2,3-b]-pyridine-5-carbonitrileHCID 69316699—

Reaction Steps

To yield compounds of structure (III) wherein R2 is carbonitrile, R3 is furan, and R1 is as defined above, intermediate 4-chloro-6-oxo-6,7-dihydro-thieno[2,3-b]pyridine-5-carbonitrile, depicted by formula (50), was reacted with 1-(2-furyl)-piperazine to yield 4-[4-(furan-2-carbonyl)-piperazin-1-yl]-6-oxo-6,7-dihydro-thieno[2,3-b]-pyridine-5-carbonitrile, depicted by formula (52). This intermediate was either reacted with an appropriate halide (R1—X) or boronic acid (R1—B(OH)2) to yield target compounds of structure (III) with R2 as carbonitrile, R3 as furan, and R1 as defined above, as shown in Scheme 27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365200B2
Source datasetuspto-grants-2008_04
ORD IDord-c44a93c34f4e4502a1007685c5212542
Source noteuspto-grants-2008_04