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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 60234생성일: 2026년 10월 25일

Cesium carbonate → Tert-butyl (6-chloro-5-fluoropyridin-3-yl)carbamate

https://huagongshe.com/reaction/60234

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물tert-Butyl carbamateHCID 77922—
반응물5-Bromo-2-chloro-3-fluoropyridineHCID 2763285—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Tris(dibenzylideneacetone) dipalladiumHCID 9832798—
용매1,4-DioxaneHCID 31275—
생성물Tert-butyl (6-chloro-5-fluoropyridin-3-yl)carbamateHCID 8665604086%

반응 조건

온도85 °C

반응 단계

A degassed mixture of 5-bromo-2-chloro-3-fluoropyridine (22.5 g, 107 mmol), tert-butyl carbamate (13.8 g, 117.5 mmol), tris(dibenzylideneacetone) dipalladium(0) (2.95 g, 3.2 mmol), XantPhos (2.48 g, 4.28 mmol) and cesium carbonate (69.7 g, 214 mmol) in dioxane (340 mL) was heated at 85° C. for 24 hours. The reaction mixture was cooled to ambient temperature and the resultant solid was removed by filtration. The resultant solid was washed with ethyl acetate followed by dichloromethane and the filtrate was combined and concentrated in-vacuo to afford a residue that was purified by flash chromatography (silica: cyclohexane to 25% ethyl acetate/cyclohexane) to afford the title compound as a pale yellow solid (22.6 g, 86%). 1H NMR (300 MHz, CDCl3): 8.04 (dd, J=10.1, 2.4 Hz, 1H), 7.98 (d, J=2.4 Hz, 1H), 6.62 (s, 1H), 1.53 (s, 9H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09440976B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-2aad88eff7364f1f9f9968439896e0fc
출처 메모uspto-grants-2016_09