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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010668Generated: October 31, 2026

1-(7-Bromo-5-pyridin-3-yl-benzothiazol-2-yl)-3-ethyl-urea → 1-(7-Allyl-5-pyridin-3-yl-benzothiazol-2-yl)-3-ethyl-urea

https://huagongshe.com/reaction/1010668

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(7-Bromo-5-pyridin-3-yl-benzothiazol-2-yl)-3-ethyl-ureaHCID 24864217—
ReactantTributylallyltinHCID 86589045—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product1-(7-Allyl-5-pyridin-3-yl-benzothiazol-2-yl)-3-ethyl-ureaHCID 57813623—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 1-(7-bromo-5-pyridin-3-yl-benzothiazol-2-yl)-3-ethyl-urea (0.14 g, 0.37 mmol) in DMF (2 mL) was added tributylallyltin (0.15 g, 0.45 mmol) under nitrogen atmosphere at room temperature. The reaction mixture was then degassed for half an hour followed by the addition of tetrakis(triphenylphosphine)palladium(0) (0.043 g, 0.0371 mmol). The reaction mixture was then again degassed for half an hour and heated at 120° C. for 20 h under nitrogen atmosphere. After the completion of the reaction (TLC monitoring), DMF was distilled off; water was added to the reaction mixture and extracted with ethyl acetate (×3). The combined organic layer was dried over anhydrous Na2SO4, and evaporated to dryness under reduced pressure. The crude residue was purified over silica gel (230-400 M) using EtOAc-MeOH (95:5) to provide the title compound as off white solid (0.034 g, 27%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977340B2
Source datasetuspto-grants-2011_07
ORD IDord-45436e08fc68496abd8a942bd8187616
Source noteuspto-grants-2011_07