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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171207Generated: November 2, 2026

Stannane, tributyl(methoxymethyl)- → HCID 57608271, compound

https://huagongshe.com/reaction/1171207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannane, tributyl(methoxymethyl)-HCID 11088958—
ReactantHCID 57608187HCID 57608187—
CatalystTetrabutylammonium ChlorideHCID 70681—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 57608271HCID 576082716%

Reaction Conditions

Temperature135 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829585B2
Source datasetuspto-grants-2010_11
ORD IDord-7e1f6b692aab4528bf356beb12aee2b3
Source noteuspto-grants-2010_11