HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 178487321, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | HCID 71278776 | HCID 71278776 | — |
| Reactant | HCID 178520025 | HCID 178520025 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178487321 | HCID 178487321 | 79% |
Reaction Steps
A solution of tert-butyl 4-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yloxy)piperidine-1-carboxylate (0.019 g, 0.052 mmol) in methanol (2.0 mL) was added with 1H-indazole-3-carboxaldehyde (0.008 g, 0.057 mmol). Then, the mixture was added with 5 drops of piperidine, and the mixture was stirred at room temperature for 2 hours. The reaction mixture was added with toluene, the solvent was evaporated under reduced pressure, and then the residue was purified by silica gel column chromatography (eluted with hexane/ethyl acetate (2:1→1:4)) to obtain tert-butyl (Z)-4-{2-[(1H-indazol-3-yl)methylene]-6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yloxy}piperidine-1-carboxylate (0.020 g, 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09156827B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-bfa63a76756f4774989418ad7bd7911b |
| Source note | uspto-grants-2015_10 |