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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1044012Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1044012

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-Chloro-4-iodopyridin-3-amineHCID 18407040—
Edukt1-Ethynyl-1-methylcyclopropaneHCID 21590560—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelTriethylamineHCID 8471—
Produkt6-Chloro-4-((1-methylcyclopropyl)ethynyl)pyridin-3-amineHCID 5790819253%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08563573B2
Quelldatensatzuspto-grants-2013_10
ORD IDord-f3f87881eed3484082014f791528b3ae
Quellennotizuspto-grants-2013_10