HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749971Generated: October 29, 2026
tert-butyl (Z)-4-[2-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)vinyl]piperidine-1-carboxylate → HCID 178487113, compound
https://huagongshe.com/reaction/1749971
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-butyl (Z)-4-[2-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)vinyl]piperidine-1-carboxylate | HCID 86682066 | — |
| Reactant | HCID 178520025 | HCID 178520025 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178487113 | HCID 178487113 | 77.2% |
Reaction Steps
A solution of tert-butyl (Z)-4-[2-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)vinyl]piperidine-1-carboxylate (0.0374 g, 0.100 mmol) in methanol (3 mL) was added with 1H-indazole-3-carboxaldehyde (0.0146 g, 0.100 mmol) and piperidine (5 drops), and the mixture was stirred at 60° C. for 2 hours. The reaction mixture was concentrated, and the resulting residue was purified by silica gel column chromatography (chloroform/methanol) to obtain tert-butyl 4-((Z)-2-{(Z)-2-[(1H-indazol-3-yl)methylene]-6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl}vinyl)piperidine-1-carboxylate (0.0387 g, 77%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09156827B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-62629f3637c648e3a448eaf02e735dbe |
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| Source note | uspto-grants-2015_10 |
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