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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642338Generated: October 30, 2026

Methallyltri-n-butyltin → 7-Hydroxy-4-(2-methyl-allyl)-2-phenyl-thiazolo[4,5-c]pyridine-6-carboxylic acid ethyl ester

https://huagongshe.com/reaction/642338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethallyltri-n-butyltinHCID 11013379—
Reactant4-Bromo-7-hydroxy-2-phenyl-thiazolo[4,5-c]pyridine-6-carboxylic acid ethyl esterHCID 86617354—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product7-Hydroxy-4-(2-methyl-allyl)-2-phenyl-thiazolo[4,5-c]pyridine-6-carboxylic acid ethyl esterHCID 6842835445.1%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 4-bromo-7-hydroxy-2-phenyl-thiazolo[4,5-c]pyridine-6-carboxylic acid ethyl ester (301.5 mg, 0.80 mmole), methallyltri-n-butyltin (529 μl, 1.60 mmole) and bis(triphenylphosphine)palladium(II) dichloride (56 mg, 0.08 mmole) in dimethylformamide (4 ml) was stirred at 130° C. for 45 min before it was cooled to room temperature, quenched with water, filtered. The filtrate was partitioned between ethyl acetate and water. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a gradient of ethyl acetate and hexanes to give the title compound as a white solid (128 mg). MS: (+) m/z 355.02 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696223B2
Source datasetuspto-grants-2010_04
ORD IDord-cbd6dcb9917e44918137ac454b1f77f7
Source noteuspto-grants-2010_04