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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 406498생성일: 2026년 10월 23일

Cesium carbonate → tert-butyl 4-(2-amino-3-nitrophenyl)-5,6-dihydropyridine-1(2H)-carboxylate

https://huagongshe.com/ko/reaction/406498

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물2-Chloro-6-nitroanilineHCID 69855—
반응물Tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,6-tetrahydropyridine-1-carboxylateHCID 4642098—
반응물Tri-t-butylphosphine fluoroborateHCID 44558591—
용매WaterHCID 962—
용매HeptaneHCID 8900—
용매1,4-DioxaneHCID 31275—
생성물tert-butyl 4-(2-amino-3-nitrophenyl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 6897430856.3%

반응 단계

A solution containing 2-chloro-6-nitroaniline (0.83 g, 4.8 mmol), tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate (2.97 g, 9.6 mmol), and cesium carbonate (3.13 g, 9.6 mmol) in dioxane (32 mL) and water (6 mL) was degassed with nitrogen and tris(dibenzylideneacetone)palladium(0) (0.22 g, 0.24 mmol) was added followed by the addition of tri-t-butylphosphine tetrafluoroborate (0.139 g, 0.48 mmol). The mixture was stirred at room temperature for about 20 min then heated at about 80° C. for about 18 h. The solvent was removed in vacuo and the residue was partitioned between water (40 mL) and EtOAc (50 mL). The organic phase was washed with brine (40 mL), dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography eluting with 12% EtOAc:heptane to yield the desired product as a yellow solid (0.87 g, 2.7 mmol). Rf (25% EtOAc:heptane) 0.68.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08754107B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-3078184b0df7487f8483883e0219f4f9
출처 메모uspto-grants-2014_06