HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749924Generated: October 31, 2026
HCID 71278791, compound → HCID 178480827, compound
https://huagongshe.com/reaction/1749924
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 71278791 | HCID 71278791 | — |
| Reactant | HCID 178520025 | HCID 178520025 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178480827 | HCID 178480827 | 24% |
Reaction Steps
A solution of 5-chloro-7-[(4-methylpiperazin-1-yl)methyl]benzofuran-3(2H)-one (0.12 g, 0.43 mmol) in methanol (5.0 mL) was added with 1H-indazole-3-carboxaldehyde (0.063 g, 0.43 mmol). Then, the mixture was added with 7 drops of piperidine, and then the mixture was stirred at 60° C. for 2 hours. The reaction mixture was concentrated, and then the residue was purified by silica gel column chromatography (eluted with chloroform/methanol (99:1→90:10)) to obtain (Z)-2-[(1H-indazol-3-yl)methylene]-5-chloro-7-[(4-methylpiperazin-1-yl)methyl]benzofuran-3(2H)-one (0.042 g, 24%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09156827B2 |
|---|
| Source dataset | uspto-grants-2015_10 |
|---|
| ORD ID | ord-21878bc1840843d6837a75a780cb9c0a |
|---|
| Source note | uspto-grants-2015_10 |
|---|