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HRID 513080作成日:2026年10月25日

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

https://huagongshe.com/reaction/513080

反応式

関与物質

役割名称HCID仕込み量
反応物6-Chloro-4-iodopyridin-3-amineHCID 18407040—
反応物1-Ethynyl-1-methylcyclopropaneHCID 21590560—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418476HCID 178418476—
溶媒TriethylamineHCID 8471—
生成物6-Chloro-4-((1-methylcyclopropyl)ethynyl)pyridin-3-amineHCID 5790819253%

反応手順

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, 2 H) 0.76 (t, J=2.4, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09102672B2
出典データセットuspto-grants-2015_08
ORD IDord-380b977ba64f4f94a05a18fe0af63e84
出典メモuspto-grants-2015_08