HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749910Generated: October 31, 2026
HCID 71278662, compound → HCID 178498961, compound
https://huagongshe.com/reaction/1749910
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 71278662 | HCID 71278662 | — |
| Reactant | HCID 178520025 | HCID 178520025 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178498961 | HCID 178498961 | 80.3% |
Reaction Steps
A solution of methyl 6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-carboxylate (0.070 g, 0.32 mmol) in methanol (5.0 mL) was added with 1H-indazole-3-carboxaldehyde (0.046 g, 0.32 mmol). Then, the mixture was added with 7 drops of piperidine, then the mixture was stirred at room temperature for 2 hours, and the solid formed was collected by filtration to obtain the objective substance. Further, the filtrate was concentrated, and then the residue was subjected to silica gel column chromatography (eluted with chloroform/methanol (97:3→90:10)) to obtain the objective substance. Two portions of the objective substance was combined to obtain 0.090 g (80%) of methyl (Z)-2-[(1H-indazol-3-yl)methylene]-6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-carboxylate.
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-890ba2018ae24504b53b6c6f13d0570f |
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| Source note | uspto-grants-2015_10 |
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