HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579190Generated: November 1, 2026
Dibutyltin dichloride → 3-(1-Cyclohexyl-4-ethoxycarbonyl-butylamino)-5-phenyl-thiophene-2-carboxylic acid methyl ester
https://huagongshe.com/reaction/579190
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dibutyltin dichloride | HCID 12688 | — |
| Reactant | Phenylsilane | HCID 12752 | — |
| Reactant | Methyl 3-amino-5-phenylthiophene-2-carboxylate | HCID 700562 | — |
| Reactant | Ethyl 5-cyclohexyl-5-oxovalerate | HCID 24727429 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-(1-Cyclohexyl-4-ethoxycarbonyl-butylamino)-5-phenyl-thiophene-2-carboxylic acid methyl ester | HCID 66684774 | 15.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040690B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-913d4c4d0c9443fa82c38552d7f49b8d |
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| Source note | uspto-grants-2015_05 |
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