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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1513237생성일: 2026년 10월 25일

2,6-Dichloro-4-morpholin-4-YL-benzaldehyde → 6-[5-(4-Chloro-phenyl)-[1,3,4]oxadiazol-2-yl]-2-(2,6-dichloro-4-morpholin-4-yl-phenyl)-1H-benzoimidazole

https://huagongshe.com/reaction/1513237

반응식

참여 물질

역할이름HCID투입량
반응물2,6-Dichloro-4-morpholin-4-YL-benzaldehydeHCID 7148605—
반응물4-[5-(4-Chloro-phenyl)-[1,3,4]oxadiazol-2-yl]-benzene-1,2-diamineHCID 66966435—
용매Dimethyl SulfoxideHCID 679—
생성물6-[5-(4-Chloro-phenyl)-[1,3,4]oxadiazol-2-yl]-2-(2,6-dichloro-4-morpholin-4-yl-phenyl)-1H-benzoimidazoleHCID 25235901—

반응 단계

To a 50 ml rbf was added 0.2250 g (0.785 mmol) 4-[5-(4-Chloro-phenyl)-[1,3,4]oxadiazol-2-yl]benzene-1,2-diamine, 0.2041 g (0.785 mmol) of 2,6-Dichloro-4-morpholin-4-yl-benzaldehyde, and 5 mL of DMSO. To this dark brown solution was added 0.0190 g (0.118 mmol) of FeCl3. It was allowed to stir open to air for 18 h. The crude was then extracted with EtOAc, and the combined extracts were washed with water, brine and dried with Na2SO4. The volatiles were removed in vacuo and the concentrate was purified on silica gel (ACN/DCM, 1:9 to 10:0) to give the title compound. 1H NMR (400 MHz, DMSO-d6) δ ppm 3.30 (d, J=5.05 Hz, 4 H) 3.71-3.77 (m, 4 H) 7.17 (s, 2 H) 7.70-7.75 (m, 2 H) 7.90 (d, J=8.72 Hz, 1 H) 7.99-8.07 (m, 1 H) 8.19 (d, J=8.21 Hz, 2 H) 8.27 (br. s., 1 H) 8.47 (s, 1 H) 13.17 (d, J=8.97 Hz, 1H. MS (m/z) 528.0 M (+1), tR=1.41, Meth 10

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08217065B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-52fab5bf56004a1586513fc5b54d2140
출처 메모uspto-grants-2012_07