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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 513080생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/513080

반응식

참여 물질

역할이름HCID투입량
반응물6-Chloro-4-iodopyridin-3-amineHCID 18407040—
반응물1-Ethynyl-1-methylcyclopropaneHCID 21590560—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매TriethylamineHCID 8471—
생성물6-Chloro-4-((1-methylcyclopropyl)ethynyl)pyridin-3-amineHCID 5790819253%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09102672B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-380b977ba64f4f94a05a18fe0af63e84
출처 메모uspto-grants-2015_08