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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579190Generated: October 31, 2026

Dibutyltin dichloride → 3-(1-Cyclohexyl-4-ethoxycarbonyl-butylamino)-5-phenyl-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/579190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibutyltin dichlorideHCID 12688—
ReactantPhenylsilaneHCID 12752—
ReactantMethyl 3-amino-5-phenylthiophene-2-carboxylateHCID 700562—
ReactantEthyl 5-cyclohexyl-5-oxovalerateHCID 24727429—
Solvent1,4-DioxaneHCID 31275—
Product3-(1-Cyclohexyl-4-ethoxycarbonyl-butylamino)-5-phenyl-thiophene-2-carboxylic acid methyl esterHCID 6668477415.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A flask was charged with 3-amino-5-phenyl-thiophene-2-carboxylic acid methyl ester (515 mg, 2.2 mmol, 1.0 equiv), 5-cyclohexyl-5-oxo-pentanoic acid ethyl ester (500 mg, 2.2 mmol, 1.0 equiv), phenyl silane (240 mg, 2.2 mmol, 1.0 equiv), dibutyltin dichloride (67 mg, 0.22 mmol, 0.1 equiv) and dioxane (2.0 mL). The resulting solution was heated at 120° C. with microwave for 2 hours. The solution was then concentrated and the residue was purified by silica gel column chromatography, EtOAc/heptane 5% to 40%, to give oil that contained starting material. The material was further purified with silica gel column chromotography, EtOH/DCM 2% to 10% to give product 150 mg (yield 15%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040690B2
Source datasetuspto-grants-2015_05
ORD IDord-913d4c4d0c9443fa82c38552d7f49b8d
Source noteuspto-grants-2015_05