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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1519919Generated: November 4, 2026

2-(Tributylstannyl)-1,3-thiazole → HCID 68754553, compound

https://huagongshe.com/reaction/1519919

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)-1,3-thiazoleHCID 2763259—
Reactant4-Bromo-5-nitrothiophene-3-carbonitrileHCID 59168810—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 68754553HCID 6875455336.1%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 4-bromo-5-nitrothiophene-3-carbonitrile (0.5 g, 2.1 mmol), 2-(tributylstannyl)thiazole (1.2 g, 3.2 mmol), dioxane (3.5 mL), and tetrakis(triphenylphosphine)palladium(0) (0.23 g, 0.21 mmol) was heated by microwave to 130° C. for 30 min under nitrogen. The reaction mix was concentrated under reduced pressure, and the resulting dark oil was purified by column chromatography using a mobile phase of 20% EtOAc/hexanes to give 5-nitro-4-(thiazol-2-yl)thiophene-3-carbonitrile (180 mg) as an oil. LCMS of this material revealed an m/z of 238.0 with a retention time of 1.807 min method [1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073891B2
Source datasetuspto-grants-2015_07
ORD IDord-30bcaaeb6ede40e2b7cc1183702c1ae6
Source noteuspto-grants-2015_07