HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 24949734, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | alpha-Chlorobenzylidenemalononitrile | HCID 176977 | — |
| Reactant | 1-(1H-Indol-3-yl)-2-(1-piperazinyl)-1,2-ethanedione | HCID 22888187 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 24949734 | HCID 24949734 | — |
Reaction Steps
Triethyl amine (1 ml) was added into a solution of 1-(1H-indol-3-yl)-2-(piperazin-1-yl)ethane-1,2-dione (150 mg) and 2-(chloro(phenyl)methylene)malononitrile (110 mg) in EtOH (20 ml). After 16 hours at 115° C., the reaction mixture was cooled down. Then the solvents were removed to offer a residue which was purified using Shimadzu automated preparative HPLC System to afford 2-((4-(2-(1H-indol-3-yl)-2-oxoacetyl)piperazin-1-yl)(phenyl)methylene)malononitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504399B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-2fb5853c35e0466c892e595cb8d83626 |
| Source note | uspto-grants-2009_03 |