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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132606생성일: 2026년 10월 26일

1,4-Dioxane → 1-(2-(2-tert-Butylphenoxy)-5-cyanopyridin-3-yl)-3-(4-tert-butylphenyl)urea

https://huagongshe.com/reaction/132606

반응식

참여 물질

역할이름HCID투입량
반응물1,4-DioxaneHCID 31275—
반응물5-Amino-6-(2-tert-butylphenoxy)nicotinonitrileHCID 68530043—
반응물HCID 178418546HCID 178418546—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
촉매Tetraethylammonium cyanideHCID 3014735—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매Diethyl EtherHCID 3283—
생성물1-(2-(2-tert-Butylphenoxy)-5-cyanopyridin-3-yl)-3-(4-tert-butylphenyl)ureaHCID 11554038—

반응 조건

온도105 °C

반응 단계

5-Amino-6-(2-tert-butylphenoxy)nicotinonitrile: A mixture of 63c (676 mg, 2.1 mmol), copper (1) cyanide (755 mg, 8.4 mmol), tris(dibenzilideneacetone)dipalladium(0) (77 mg, 0.08 mmol), bis(diphenylphosphino)ferrocene (187 mg, 0.34 mmol) and tetraethylammonium cyanide (330 mg, 2.1 mmol) in dioxane (11 mL) was heated at 105° C. overnight. The mixture was cooled to rt, diluted with ether (50 mL), filtered through Celite® and silica (3 g) and concentrated to give a brown solid (883 mg). The solid was purified by SiO2 chromatography (40 g) to afford 63d (472 mg. 84% yield) as a yellow solid; HPLC purity 95%, 3.37 min (Method A); [M+H]+=268.15; 1H NMR (CDCl3) δ ppm: 1.35 (s, 9 H) 4.26 (s, 2 H) 6.95 (d, J=7.70 Hz, 1 H) 7.15 (s, 1 H) 7.20 (t, J=7.70 Hz, 1 H) 7.25 (t, J=7.42 Hz, 1 H) 7.47 (d, J=7.70 Hz, 1 H) 7.82 (s, 1 H); 13C NMR (CDCl3) δ ppm: 154.22, 151.27, 141.40, 139.75, 131.98, 127.57, 127.03, 125.53, 123.53, 121.69, 117.38, 104.08, 34.60, 30.47.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388021B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-901db812d251499d9e832bd475385333
출처 메모uspto-grants-2008_06