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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447016Generated: October 29, 2026

Potassium Phosphate, Tribasic → HCID 24864398, compound

https://huagongshe.com/reaction/447016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant3-Pyridinylboronic acidHCID 2734378—
ReactantHCID 57813627HCID 57813627—
CatalystHCID 178418476HCID 178418476—
SolventN,N-Dimethylformamide--water (1/1)HCID 21962138—
ProductHCID 24864398HCID 2486439824.5%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 1-(7-bromo-5-pyrazol-1-yl-benzothiazol-2-yl)-3-ethyl-urea (0.27 g, 0.74 mmol) in DMF: H2O (2:1, 15 mL) was added 3-pyridyl boronic acid (0.11 g, 0.88 mmol) and K3PO4 (0.17 g, 0.81 mmol) under nitrogen atmosphere at room temperature. The reaction mixture was then degassed for half an hour followed by the addition of bis(triphenylphosphine)palladium(II) dichloride (0.077 g, 0.11 mmol). The reaction mixture was then again degassed for half an hour and heated at 120° C. for 2 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. The combined organic layers were dried over anhydrous Na2SO4, and evaporated to dryness under reduced pressure. The crude residue was purified over silica gel (230-400 M) using EtOAc-Hexane (70:30) to provide the title compound (0.066 g, 22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481544B2
Source datasetuspto-grants-2013_07
ORD IDord-15106e975221472190fdc3e6e6d274fe
Source noteuspto-grants-2013_07