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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1044012Generated: October 25, 2026

6-Chloro-4-iodopyridin-3-amine → 6-Chloro-4-((1-methylcyclopropyl)ethynyl)pyridin-3-amine

https://huagongshe.com/reaction/1044012

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloro-4-iodopyridin-3-amineHCID 18407040—
Reactant1-Ethynyl-1-methylcyclopropaneHCID 21590560—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
Product6-Chloro-4-((1-methylcyclopropyl)ethynyl)pyridin-3-amineHCID 5790819253%

Reaction Steps

To a solution of 6-chloro-4-iodopyridin-3-amine (7.0 g, 28 mmol) in Et3N (100 mL) was added 1-ethynyl-1-methyl-cyclopropane (11.0 g, 137 mmol), CuI (0.53 g, 2.8 mmol) and Pd(PPh3)2Cl2 (1.9 g, 2.8 mmol) under N2 atmosphere. The mixture was refluxed overnight and quenched with H2O (100 mL). The organic layer was separated and the aqueous layer was extracted with ethyl acetate (100 mL×3). The combined organic layers were washed with brine, dried over anhydrous Na2SO4 and purified by chromatography on silica gel (3% EtOAc in Petroleum ether as eluant) to afford 6-chloro-4-((1-methylcyclopropyl)ethynyl)pyridin-3-amine (3.0 g, 53%). 1H-NMR (CDCl3, 300 MHz) δ 7.84 (s, 1H), 7.08 (s, 1H), 4.11 (br s, 2H), 1.37 (s, 3H), 1.03 (t, J=2.4, 2H) 0.76 (t, J=2.4, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563573B2
Source datasetuspto-grants-2013_10
ORD IDord-f3f87881eed3484082014f791528b3ae
Source noteuspto-grants-2013_10