HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171207Generated: November 2, 2026
Stannane, tributyl(methoxymethyl)- → HCID 57608271, compound
https://huagongshe.com/reaction/1171207
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stannane, tributyl(methoxymethyl)- | HCID 11088958 | — |
| Reactant | HCID 57608187 | HCID 57608187 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 57608271 | HCID 57608271 | 6% |
Reaction Steps
To a 1-methyl-2-pyrrolidinone (500 μL) solution of trifluoromethanesulfonic acid 2-(((2-amino-6-methoxymethyl-pyridin-3-carbonyl)-amino)-methyl)-benzofuran-6-yl ester (15 mg, 33 μmol) described in Production Example 47-1 were added tributyl-methoxymethyl-stannane (14 mg, 43 μmol), tetrakis(triphenylphosphine)palladium (0) (3.78 mg, 3.3 μmol) and tetrabutyl ammonium chloride (1.82 mg, 6.5 μmol) at room temperature, which was stirred at 135° C. for 4 hours under nitrogen atmosphere. After allowing the reaction solution to cool to room temperature, the reaction solution was filtered and purified by reverse phase high-performance liquid chromatography (using an acetonitrile-aqueous mobile phase (containing 0.1% trifluoroacetic acid)) followed by further purifying by silica gel column chromatography (ethyl acetate) to obtain the title compound (0.7 mg, 6%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07829585B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-7e1f6b692aab4528bf356beb12aee2b3 |
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| Source note | uspto-grants-2010_11 |
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