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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969525Generated: November 3, 2026

Sodium Carbonate → HCID 58009875, compound

https://huagongshe.com/reaction/1969525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantStyrylboronic acidHCID 5702628—
Reactant2-Bromo-5-((4-methylphenyl)sulfonyl)-5H-pyrrolo(2,3-b)pyrazineHCID 52987643—
CatalystHCID 178418807HCID 178418807—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58009875HCID 5800987536.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 2-bromo-5-tosyl-5H-pyrrolo[2,3-b]pyrazine (3.1 g, 8.8 mmol, Example #1, Step B), PdCl2(dppf)•DCM (0.719 g, 0.880 mmol) and (E)-styrylboronic acid (2.60 g, 17.6 mmol) in THF (3 mL) and water (2 mL) was added Na2CO3 (2.33 g, 22.0 mmol). The reaction mixture was degassed with argon for about 5 min. The reaction mixture was heated at about 50° C. After about 24 h, additional PdCl2(dppf)•DCM (0.719 g, 0.880 mmol), (E)-styrylboronic acid (2.60 g, 17.6 mmol) and Na2CO3 (2.33 g, 22.0 mmol) were added to the reaction mixture. After heating at about 50° C. for about 48 h, the reaction mixture was cooled to ambient temperature and diluted with DCM (200 mL) and water (200 mL). The organic layer was separated, dried over anhydrous Na2SO4, filtered, and coned under reduced pressure. Purification by chromatography over silica gel eluting with a gradient of 20-60% EtOAc in heptane containing 5% DCM provided (E)-2-styryl-5-tosyl-5H-pyrrolo[2,3-b]pyrazine as a yellow solid (1.2 g, 36%): LC/MS (Table 1, Method a) Rt=2.99 min; MS m/z: 376 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426411B2
Source datasetuspto-grants-2013_04
ORD IDord-d4ad8bc04a6b4b2fb29345d9d7247905
Source noteuspto-grants-2013_04