HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743353Generated: October 30, 2026
HCID 11011683, compound → HCID 9967388, compound
https://huagongshe.com/reaction/1743353
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 11011683 | HCID 11011683 | — |
| Reactant | 1-Benzyl-3-iodoindazole | HCID 11067603 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 9967388 | HCID 9967388 | 69% |
Reaction Steps
A solution of methyl 5-bromofuranoate (0.75 g, 3.66 mmol), hexamethylditin (1.0 g, 3.05 mmol) and Pd(PPh3)4 (90 mg, 0.078 mmol) in DME (50 mL) was heated to reflux overnight. The initial amber coloured solution became black. The solution was allowed to cool and then filtered and concentrated under reduced pressure. The crude stannane was purified by passage through a plug of silica (1:9 EtOAc:cyclohexane) to give methyl 2-trimethylstannyl-5-furanoate (0.17 g, 19%): 1H-NMR (CDCl3); The low yield of the product may be due to its suspected volatility. Pd(PPh3)4 (9 mg, 0.008 mmol) was added to a solution of 1-benzyl-3-iodo-1H-indazole (0.13 g, 0.39 mmol) and methyl 2-trimethylstannyl-5-furanoate (0.17 g, 0.588 mmol) in DME (20 mL).and the mixture was heated to reflux overnight. The reaction mixture was allowed to cool to rt, filtered and concentrated under reduced pressure. Purification of the residue by chromatography on silica (3:7 EtOAc:cyclohexane) gave the product as a slightly contaminated yellow solid (88.6 mg, 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07009056B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-bb5cb2caec4e43edb84c3d7ba6446247 |
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| Source note | uspto-grants-2006_03 |
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