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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2183458생성일: 2026년 10월 24일

Pyridine → (S)-{1-[3-(6-Methyl-pyridin-3-yloxy)-phenyl]-ethyl}-carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/2183458

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Potassium CarbonateHCID 11430—
반응물2-Methyl-5-hydroxypyridineHCID 14275—
반응물(S)-N-Boc-1-(3-bromophenyl)ethylamineHCID 56971804—
촉매Copper iodideHCID 83717—
용매TriethylamineHCID 8471—
용매Ethyl AcetateHCID 8857—
생성물(S)-{1-[3-(6-Methyl-pyridin-3-yloxy)-phenyl]-ethyl}-carbamic acid tert-butyl esterHCID 6000412233%

반응 조건

온도145 °C

반응 단계

A mixture of (S)-[1-(3-bromo-phenyl)-ethyl]-carbamic acid tert-butyl ester (10 g, 33.3 mol), 5-hydroxy-2-methylpyridine (4 g, 36.7 mol), copper iodide (6.3 g, 33.3 mol), potassium carbonate (9.2 g, 66.7 mol) and pyridine (33 mL) in sealed tube was heated at 145° C. for six days. The reaction was cooled down to room temperature and filtered, the filtrate was washed with H2O and extracted with CH2Cl2 three times, and the combined organic layers were dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with 30:20:1/Hexane:EtOAc:triethylamine to give the title product (3.8 g, 33% yield) as sticky yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06900210B2
출처 데이터셋uspto-grants-2005_05
ORD IDord-0bf77f5291be4eca96399512bad071f4
출처 메모uspto-grants-2005_05