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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708295Generated: October 29, 2026

(Z)-1-Ethoxy-2-(tributylstannyl)ethene → HCID 58203696, compound

https://huagongshe.com/reaction/708295

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Z)-1-Ethoxy-2-(tributylstannyl)etheneHCID 2763294—
Reactant8-Bromo-2-(2-isopropyl-5-methyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azuleneHCID 58203908—
CatalystHCID 178418476HCID 178418476—
ProductHCID 58203696HCID 5820369663%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 8-bromo-2-(2-isopropyl-5-methyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene (0.220 g, 0.000543 mol), tributyl-ethoxyvinyl-tin (0.202 mL, 0.000597 mol), and bis(triphenylphosphine)palladium(II) chloride (0.0190 g, 0.0271 mmol) was degassed with N2. The reaction was heated to 100° C. overnight. The crude was hydrolyzed with 10% HCl and extracted 3 times with ethyl acetate. The organic layers were combined, dried with MgSO4 and concentrated. The crude was loaded as a solid onto silica and purified by flash chromatography (45-100% ethyl acetate in hexanes) to give 1-[2-(2-Isopropyl-5-methyl-2H-[1,2,4]triazol-3-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulen-8-yl]-ethanone as a white solid (126 mg). MS(ESI+) 369.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09175009B2
Source datasetuspto-grants-2015_11
ORD IDord-c7b9e66952344e0c9262be4cdadb3df9
Source noteuspto-grants-2015_11