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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233079Generated: October 31, 2026

Water → HCID 57438740, compound

https://huagongshe.com/reaction/2233079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantTri-t-butylphosphine fluoroborateHCID 44558591—
Reactant8-Chloro-2-(4-fluorophenyl)imidazo[1,2-A]pyrazineHCID 57438741—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57438740HCID 57438740642.6%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a mixture of 8-chloro-2-(4-fluorophenyl)-imidazo[1,2-a]pyrazine (Example #6, Step A, 3.96 g, 16 mmol) in dioxane (80 mL) was added water (15.4 mL), sodium carbonate (EM Science, 5.08 g, 48 mmol), tri-t-butylphosphine tetrafluoroborate (Strem, 0.46 g, 1.6 mmol), and tris(dibenzylideneacetone)dipalladium(0) (0.73 g, 0.8 mmol). The reaction was degassed with nitrogen and then vinylboronic acid pinacolester (5.44 mL, 32 mmol) was added. The mixture was heated to about 95° C. for about 16 h. The reaction was cooled, EtOAc was added (250 mL), and the mixture was washed with water. The organic layer was dried over sodium sulfate, filtered, and evaporated. The residue was purified by FCC (33%-50% EtOAc/heptane). The residue was triturated with heptane and filtered to yield the title compound as a brown solid (2.46 g, 62%): LC/MS (Table 1, Method b) Rt=2.74 min; MS m/z: 240.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709468B2
Source datasetuspto-grants-2010_05
ORD IDord-c81084fa5c8e49cd97f9962520398057
Source noteuspto-grants-2010_05