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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854601Generated: October 30, 2026

Potassium Carbonate → HCID 53312330, compound

https://huagongshe.com/reaction/1854601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantThiophene-3-boronic acidHCID 581760—
ReactantHCID 67324626HCID 67324626—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53312330HCID 5331233089%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of [6-(2-chloro-oxazol-5-yl)-pyridin-2-yl]-(5-chloro-pyridin-2-yl)-amine (50 mg, 0.162 mmol) in THF (4 ml) and water (2 ml) was treated with 3-thiopheneboronic acid (25 mg, 0.195 mmol), Pd(PPh3)4 (19 mg, 0.0162 mmol) and K2CO3 (50 mg, 0.358 mmol) before heating to 100° C. for 60 h. The cooled mixture was treated with water and extracted with DCM. The combined organics were dried over MgSO4, filtered and evaporated under reduced pressure before purification by column chromatography on SiO2, eluting with 1% EtOH in DCM to afford the title compound as an off-white solid (51 mg, 89%). 1H NMR (400 MHz, DMSO-d6) δ 10.05 (s, 1H), 8.33-8.31 (m, 1H), 8.28 (d, J=2.5 Hz, 1H), 8.15 (d, J=9.0 Hz, 1H), 7.89 (dd, J=9.0, 2.7 Hz, 1H), 7.85 (s, 1H), 7.83-7.77 (m, 2H), 7.69-7.65 (m, 1H), 7.49 (d, J=8.3 Hz, 1H), 7.40 (d, J=7.4 Hz, 1H). (ESI+) m/z 355 (M+H)+. Retention time=4.28 mins (method 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962665B2
Source datasetuspto-grants-2015_02
ORD IDord-b0ab1c26e3aa40b0b6d0052fb3ae0949
Source noteuspto-grants-2015_02