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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 561029Generated: November 1, 2026

Sodium Bicarbonate → HCID 86640496, compound

https://huagongshe.com/reaction/561029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
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—
Reactant5-Azidomethyl-2-fluoro-4-iodo-pyridineHCID 86640490—
CatalystPalladium ChlorideHCID 24290—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 86640496HCID 86640496100%

Reaction Conditions

Temperature85 °C

Reaction Steps

Combine 5-azidomethyl-2-fluoro-4-iodo-pyridine (70 mg, 0.25 mmol) and 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 (100 mg, 0.21 mmol) bis(diphenylphosphino)ferrocene)dichloro palladium (8.5 mg, 0.01 mmol) and NaHCO3 (35 mg, 0.41 mmol) in DMSO (87 mL) and water (3 mL). Purge the mixture through nitrogen for 5 min twice. Heat the mixture at 85° C. for 1 hour in an oil bath. Cool to room temperature. Dilute the reaction mixture with chloroform/isopropyl alcohol 93/1), and wash with water and saturated aqueous sodium chloride. Separate the organic layer from the aqueous layer and dry over sodium sulfate. After filtration, remove the organic solvent to give a crude mixture. Purify the crude by column chromatography (10% methanol in dichloromethane) to afford the title compound (105 mg, 100%). MS (ES) m/z 508 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063212B2
Source datasetuspto-grants-2011_11
ORD IDord-1344b220f4cb41ff8c7a934d0ab9a197
Source noteuspto-grants-2011_11