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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426985Generated: October 30, 2026

Potassium Carbonate → HCID 59232734, compound

https://huagongshe.com/reaction/2426985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
ReactantHCID 59232719HCID 59232719—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
ProductHCID 59232734HCID 5923273440.3%

Reaction Steps

An Emry™ process vial was charged with 3-(4-bromo-phenyl)-2,2-dimethyl-3-phenyl-N-thiazol-2-yl-propionamide (70 mg, 0.168 mmol) and 4-methoxy-phenylboronic acid (77 mg, 0.50 mmol), tetrakis(triphenylphosphine)palladium(0) (20 mg, 0.017 mmol), 2.0 mL of 2M K2CO3, and 1.5 mL of DMF. The reaction mixture was degassed by bubbling nitrogen through for 15 min, then sealed and exposed to microwave irradiation for 30 min at 150° C. The reaction mixture was cooled, filtered, and diluted with ethyl acetate. The organic solution was washed, dried and concentrated. The crude product was purified by preparative HPLC to give the title compound of Example 374 as a white solid (30 mg, 40%). LC/MS (m/z) 444.37 [(M+H)+]; HPLC Rt: 3.770 min. 1H NMR (400 MHz, MeOD) δ ppm 7.34-7.54 (9H, m) 7.23 (2H, t, J=7.38 Hz) 7.16 (1H, t, J=7.12 Hz) 7.02 (1H, d, J=3.56 Hz) 6.93 (2H, d, J=8.65 Hz) 4.63 (1H, s) 3.78 (3H, s) 1.40 (6H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968577B2
Source datasetuspto-grants-2011_06
ORD IDord-0a8f26f33cef48798a6acc62781ee60c
Source noteuspto-grants-2011_06