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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227233Generated: October 30, 2026

3-Bromopyridine → HCID 69052614, compound

https://huagongshe.com/reaction/227233

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromopyridineHCID 12286—
Reactant875768-16-4HCID 50998820—
CatalystHCID 178418476HCID 178418476—
ProductHCID 69052614HCID 69052614—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of 3-bromopyridine (608 mg, 3.85 mmol), PdCl2(PPh3)2 (246 mg, 0.35 mmol), and Cu(1)I (733 mg, 3.85 mmol) was added TEA (10 mL) followed by 1-ethynyl-4-methyl-2-nitro-benzene (564 mg, 3.5 mmol). After stirring at 60° C. for 4 h, the reaction was filtered, and diluted with EtOAc (150 mL) and 10% Na2CO3 (150 mL). The organic layer was washed with brine, dried over MgSO4; filtered, and dried under reduced pressure. The material was purified using a Biotage 40M cartridge eluting with hexanes/EtOAc (7/3) to yield a light brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560462B2
Source datasetuspto-grants-2009_07
ORD IDord-d7640c7d74c2422388ac9c0660be5fa4
Source noteuspto-grants-2009_07