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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906392Generated: October 27, 2026

3-Methylbut-1-yne → 2-Chloro-5-(3-methylbut-1-ynyl)pyridin-4-amine

https://huagongshe.com/reaction/906392

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Methylbut-1-yneHCID 69019—
Reactant2-Chloro-5-iodopyridin-4-amineHCID 45480366—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product2-Chloro-5-(3-methylbut-1-ynyl)pyridin-4-amineHCID 58025064—

Reaction Steps

To a solution of 2-chloro-5-iodopyridin-4-amine (Compound 11, 2.55 g, 10.0 mmol) in Et3N (35 ml) was added Pd(PPh3)2Cl2 (70 mg, 0.10 mmol), Cul (19 mg, 0.10 mmol), and 3-methyl-1-butyne (1.2 ml, 12 mmol). The reaction was stirred at room temperature for 20 h and was quenched with H2O, extracted with EtOAc (×2). The combined organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by chromatography on silica gel (0→30% EtOAc-hexanes) to yield the title compound as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012992B2
Source datasetuspto-grants-2011_09
ORD IDord-6f79e9709ebf4225aa22e7672e4b0170
Source noteuspto-grants-2011_09