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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271559Generated: November 3, 2026

1-Ethynyl-3-methoxybenzene → HCID 10105613, compound

https://huagongshe.com/reaction/1271559

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethynyl-3-methoxybenzeneHCID 640753—
Reactant2-Bromo-6-methylpyridin-3-amineHCID 14418051—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductHCID 10105613HCID 1010561346.7%

Reaction Steps

Following the same procedure as described in Example 1, (2-bromo-6-methyl-pyridin-3-yl)amine (200 mg, 1.07 mmol) reacted with (PPh3)2PdCl2 (37 mg, 0.05 mmol), Cul (10 mg, 0.05 mmol) and 1-ethynyl-3-methoxy-benzene (204 μl, 1.60 mmol) in triethylamine (5 ml) during 1.5 h. The crude residue was purified by flash chromatography (hexane/ethyl acetate 4:1) to yield 118 mg (0.50 mmol, 46%) of (2-(3-methoxy-phenylethynyl)-6-methyl-pyridin-3-yl)amine as a yellow brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205411B2
Source datasetuspto-grants-2007_04
ORD IDord-1c2ba9a75ebe43b8af57bd2ceb74e28c
Source noteuspto-grants-2007_04