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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 902476Generated: October 30, 2026

1-(Thien-2-ylcarbonyl)piperazine → 6-Oxo-4-[4-(thiophene-2-carbonyl)-piperazin-1-yl]-6,7-dihydro-thieno[2,3-b]pyridine-5-carbonitrile

https://huagongshe.com/reaction/902476

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Thien-2-ylcarbonyl)piperazineHCID 797562—
Reactant4-Chloro-6-oxo-6,7-dihydro-thieno[2,3-b]pyridine-5-carbonitrileHCID 59702118—
Product6-Oxo-4-[4-(thiophene-2-carbonyl)-piperazin-1-yl]-6,7-dihydro-thieno[2,3-b]pyridine-5-carbonitrileHCID 69312668—

Reaction Steps

To yield a compound of structure (III) with R2 as carbonitrile, R3 as thiophene, and R1 as defined above, the intermediate 4-chloro-6-oxo-6,7-dihydro-thieno[2,3-b]pyridine-5-carbonitrile, depicted by formula (50), was reacted with piperazin-1-yl-thiophene-2-yl-methanone to yield 6-oxo-4-[4-(thiophene-2-carbonyl)-piperazin-1-yl]-6,7-dihydro-thieno[2,3-b]pyridine-5-carbonitrile, depicted by formula (51). The compound of formula (51) was either reacted with an appropriate halide (R1—X) or boronic acid (R1—B(OH)2) to yield the target compounds of structure (III) with R2 as carbonitrile, R3 as thiophene, and R1 as defined above, as shown in Scheme 26.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07365200B2
Source datasetuspto-grants-2008_04
ORD IDord-e1601e7d3fda4f3e9c03c39374583b9d
Source noteuspto-grants-2008_04