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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099628Generated: October 25, 2026

Dibutyltin dichloride → 5-Cyclohex-1-enyl-3-[(3-oxo-octahydro-indolizin-7-yl)-amino]-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/2099628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibutyltin dichlorideHCID 12688—
ReactantPhenylsilaneHCID 12752—
ReactantHexahydroindolizine-3,7-dioneHCID 12345000—
Reactant5-Cyclohex-1-enyl-3-aminothiophene-2-carboxylic acid methyl esterHCID 57795401—
SolventTetrahydrofuranHCID 8028—
Product5-Cyclohex-1-enyl-3-[(3-oxo-octahydro-indolizin-7-yl)-amino]-thiophene-2-carboxylic acid methyl esterHCID 5779549690%

Reaction Steps

To a solution of 5-cyclohex-1-enyl-3-aminothiophene-2-carboxylic acid methyl ester (689 mg, 2.90 mmol) and 3-oxo-octahydro-indolizin-7-one (750 mg, 4.90 mmol; prepared as described in Tetrahedron, 1975, 1437) in 3 mL of dry THF was added dibutyltin dichloride (88 mg, 0.29 mmol), and the mixture was stirred for 10 min at room temperature under nitrogen. Then phenylsilane (394 μL, 3.19 mmol) was added, and the mixture was stirred overnight at room temperature. Solvent was evaporated under reduced pressure, and the residue was purified by column chromatography on silica gel using gradient 30-100% EtOAc in hexane to afford 973 mg (90%) of 5-cyclohex-1-enyl-3-[(3-oxo-octahydro-indolizin-7-yl)-amino]-thiophene-2-carboxylic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569600B2
Source datasetuspto-grants-2009_08
ORD IDord-6646f6585706467985fe887724d83850
Source noteuspto-grants-2009_08