HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 71278610, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 1-(4-Methylbenzene-1-sulfonyl)-1H-indole-3-carbaldehyde | HCID 735817 | — |
| Reactant | HCID 71278947 | HCID 71278947 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 71278610 | HCID 71278610 | 81.6% |
Reaction Steps
A solution of 6-hydroxy-7-[(4-methylpiperazin-1-yl)methyl]benzofuran-3(2H)-one (0.525 g, 2.00 mol) in methanol (10 mL) was added with 1-tosyl-1H-indole-3-carboxaldehyde (0.599 g, 2.00 mmol) and piperidine (0.017 g, 0.200 mmol), and the mixture was stirred overnight at room temperature. The reaction mixture was added with methanol, and the solid was suspended in methanol and thereby washed to obtain the objective (Z)-6-hydroxy-7-[(4-methylpiperazin-1-yl)methyl]-2-[(1-tosyl-1H-indol-3-yl)methylene]benzofuran-3(2H)-one (0.887 g, 81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09156827B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-0fb1e604da684836bd60fa143845e119 |
| Source note | uspto-grants-2015_10 |