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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17111생성일: 2026년 10월 24일

2,6-Dibromopyridine → 6-Bromo-pyridine-2-carboxylic acid tert-butylamide

https://huagongshe.com/ko/reaction/17111

반응식

참여 물질

역할이름HCID투입량
반응물2,6-DibromopyridineHCID 12274—
반응물tert-Butyl isocyanateHCID 62412—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물6-Bromo-pyridine-2-carboxylic acid tert-butylamideHCID 60133833—

반응 단계

2,6-Dibromopyridine (40 g, 170 mmol) in THF (200 mL) was added dropwise over 1 hr to a cooled (−78 C) solution of n-butyllithium (2.0M in pentane, 85 mL, 170 mmol) in THF (100 mL) under a nitrogen atmosphere. The mixture was allowed to stir for an additional 15 min, then tert-butyl isocyanate was added dropwise over 5 min. The resulting reaction mixture was allowed to warm slowly to room temperature overnight before quenching with saturated ammonium chloride solution (200 mL) and extracting with ethyl acetate (2×100 mL). The combined organics were dried (MgSO4) and evaporated in vacuo to yield the cude product A466.1 (42.4 g) as a dark brown oil which was used immediately without further purification. HPLC YMC S-5 4.6×33 mm (2 min grad): retention time 1.76 min, M+H+=203.08

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737279B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-a2e006812d4b46bbbc5094eccf2321c1
출처 메모uspto-grants-2010_06