HuagongsheHuagongshe Chemistry Print Report · For research reference only
Furan → 5-Oxo-7-[4-(furan-2-carbonyl)-piperazin-1-yl]-4,5-dihydro-2-thia-4-aza-indene-6-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Furan | HCID 8029 | — |
| Reactant | 1-(Furan-2-yl)piperazine | HCID 19763577 | — |
| Reactant | 7-Chloro-5-oxo-4,5-dihydro-2-thia-4-aza-indene-6-carbonitrile | HCID 59702077 | — |
| Product | 5-Oxo-7-[4-(furan-2-carbonyl)-piperazin-1-yl]-4,5-dihydro-2-thia-4-aza-indene-6-carbonitrile | HCID 58938220 | — |
Reaction Steps
To yield compounds of structure (II) wherein R2 is carbonitrile, R3 is furan, and R1 is as defined above, intermediate 7-chloro-5-oxo-4,5-dihydro-2-thia-4-aza-indene-6-carbonitrile, depicted by formula (33), was reacted with 1-(2-furyl)-piperazine to yield 5-oxo-7-[4-(furan-2-carbonyl)-piperazin-1-yl]-4,5-dihydro-2-thia-4-aza-indene-6-carbonitrile, depicted by formula (35). This intermediate was either reacted with an appropriate halide (R1—X) or boronic acid (R1—B(OH)2) to yield the target compounds of structure (II) with R2 as carbonitrile, R3 as furan, and R1 as defined above, as shown in Scheme 17.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07365200B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-9c6feab2f8ba4a4496dee0a81fd2f952 |
| Source note | uspto-grants-2008_04 |