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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422114Generated: October 31, 2026

Sodium Carbonate → HCID 24936343, compound

https://huagongshe.com/reaction/422114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
Reactant1-(2-{5-Fluoro-4-[7-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzo[b]thiophen-2-yl]-pyrimidin-2-ylamino}-ethyl)-imidazolidin-2-oneHCID 66673481—
ReactantHCID 66674391HCID 66674391—
Solvent1,4-DioxaneHCID 31275—
SolventChloroform isopropyl alcoholHCID 21906603—
ProductHCID 24936343HCID 2493634321%

Reaction Conditions

Temperature100 °C

Reaction Steps

Combine 1-(2-{5-fluoro-4-[7-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzo[b]thiophen-2-yl]-pyrimidin-2-ylamino}-ethyl)-imidazolidin-2-one (120 mg, 0.25 mmol), (6-fluoro-4-iodo-pyridin-3-yl)-methanol (100 mg; 0.32 mmol), (1,1′-bis(di-phenylphosphino)ferrocene)palladium(II) chloride (10.14 mg; 0.01 mmol), 2-(di-tert-butylphosphino)biphenyl (2 mg, 0.01 mmol) and sodium carbonate (2 M, 0.2 mL, 0.4 mmol) in 5 mL of dioxane in a pressure tube. Heat the mixture at 100° C. overnight in oil bath. Cool the mixture down to room temperature, dilute it with chloroform-isopropyl alcohol (3/1). Wash the organic phase with saturated aqueous sodium chloride, dry it over sodium sulfate and concentrate it to an oily residue. Purify the crude by flash column chromatography (10% methanol in dichloromethane) to afford the title compound (25 mg, 21%). MS (ES) m/z 483 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101628B2
Source datasetuspto-grants-2012_01
ORD IDord-8eafebf2920d46d4bc149d2e53ac286c
Source noteuspto-grants-2012_01