HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Thien-2-ylcarbonyl)piperazine | HCID 797562 | — |
| Reactant | 4-Chloro-6-oxo-6,7-dihydro-thieno[2,3-b]pyridine-5-carbonitrile | HCID 59702118 | — |
| Product | 6-Oxo-4-[4-(thiophene-2-carbonyl)-piperazin-1-yl]-6,7-dihydro-thieno[2,3-b]pyridine-5-carbonitrile | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07365200B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-e1601e7d3fda4f3e9c03c39374583b9d |
| Source note | uspto-grants-2008_04 |