HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749887Generated: November 1, 2026
HCID 71278867, compound → HCID 178487199, compound
https://huagongshe.com/reaction/1749887
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 71278867 | HCID 71278867 | — |
| Reactant | HCID 178520025 | HCID 178520025 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178487199 | HCID 178487199 | 85% |
Reaction Steps
A solution of tert-butyl 4-[1-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)-ethyl]piperazine-1-carboxylate (0.091 g, 0.24 mmol) in methanol (3.0 mL) was added with 1H-indazole-3-carboxaldehyde (0.039 g, 0.27 mmol). Then, the mixture was added with 5 drops of piperidine, and then the mixture was stirred at 60° C. for 1 hour. The solvent was evaporated under reduced pressure, and then the residue was subjected to silica gel column chromatography (aminopropyl silica was used, eluted with chloroform/methanol (100:0→97:3)) to obtain tert-butyl (Z)-4-(1-{2-[(1H-indazol-3-yl)methylene]-6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl}ethyl)piperazine-1-carboxylate (0.10 g, 85%).
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-21d27cd9b26841ae8e67e0cd89ad60a1 |
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| Source note | uspto-grants-2015_10 |
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