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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010648Generated: October 31, 2026

Potassium Phosphate, Tribasic → HCID 24864398, compound

https://huagongshe.com/reaction/1010648

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 numberUS07977340B2
Source datasetuspto-grants-2011_07
ORD IDord-b9e2503387ac4c17b49597c1bede7250
Source noteuspto-grants-2011_07