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HRID 1405703생성일: 2026년 10월 26일

2-Methylpyridine → 3-[(7-Methoxynaphthalen-2-yl)oxy]pyridin-2-amine

https://huagongshe.com/reaction/1405703

반응식

참여 물질

역할이름HCID투입량
반응물2-MethylpyridineHCID 7975—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물2-Amino-3-bromopyridineHCID 817700—
반응물7-Methoxy-2-naphtholHCID 853173—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물3-[(7-Methoxynaphthalen-2-yl)oxy]pyridin-2-amineHCID 6674854036.1%

반응 조건

온도140 °C

반응 단계

A mixture of picoline acid (0.427 g), tripotassium phosphate (11.04 g), copper (I) iodide (0.660 g), 7-methoxynaphthalen-2-ol (6.04 g), 3-bromopyridin-2-amine (3 g) and DMSO (50 mL) was stirred under a nitrogen atmosphere at 140° C. overnight. Water was added, and the mixture was filtered through celite, and the filtrate was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) and basic silica gel column chromatography (ethyl acetate/hexane) to give the title compound (1.667 g) as a pale-yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08916551B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-85ce27eb5aef4eafb3451ded3ad44c47
출처 메모uspto-grants-2014_12