CAS: 20555-91-3; 1,2-Dichloro-4-Iodobenzene

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CAS号95-76-1 3,4-二氯苯胺 | CAS号401797-02-2 3.4-二氯苯硼酸频呢醇酯 | CAS号95-50-1 邻二氯苯 | CAS号16156-46-0 3.4-Dichlor-ben... | CAS号3024-72-4 3,4-二氯苯甲酰氯 | CAS号38380-03-9 2,3,3',4',6-五氯联苯 | CAS号32598-14-4 2,3,3',4,4'-五氯联苯 | CAS号32598-13-3 3,3',4,4'-四氯联苯 | CAS号75403-32-6 1,3-dichloro-5-... | CAS号31508-00-6 2,3',4,4',5-五氯联苯标准溶液 | CAS号32598-10-0 2,3',4,4'-四氯联苯 | CAS号32598-11-1 2,3,4,5-四氯联苯醚 | CAS号56558-17-9 2,3',4,4',6-五氯联苯 | CAS号41464-43-1 2,3,3'4'-四氯联苯

邻二氯苯置于copper(L) Iodide,1,10-菲罗啉,(1,5-Cyclooctadiene)(Methoxy)Iridium(I) Dimer,4,4'-Di-Tert-Butyl-2,2'-Bipyridine,Potassium Iodide体系中,用 四氢呋喃,甲醇,水 用作溶剂,化学反应 25.0H,反应生成3,4-二氯碘苯
参考文献:通过铱催化的c-h硼化作用对芳烃进行立体控制的碘化
标题:通过铱催化的c-h硼化作用对芳烃进行立体控制的碘化
摘要:报道了一种通过连续的c-h硼化和碘化制备芳基和杂芳基碘化物的温和方法.该过程的区域选择性由c-h硼化步骤中的空间效应控制,是对现有形成芳基碘化物的方法的补充.硼酸酯的碘化具有放射性标记的芳基碘化物的合成潜力,正如spect成像的潜在示踪剂的简明合成所证明的那样.
Doi:10.1021/ol303164H

专利信息

专利号:WO-2017072796-A1
优先权日:2015-10-30
标题 :2-pyridone based compounds useful as potential phosphodiesterase3a (pde3a)inhibitors and a process for the preparation thereof
发明人：KUMAR G JAGADEESH; MAHENDAR B; SAIDULU M; BANERJEE S K; RAO V JAYATHIRTHA
权利人:COUNCIL SCIENT IND RES
摘要:Formula A wherein X = COOCH 3 , COOC 2 H 5 , CN Y = Methyl, Phenyl R = alkyl, substituted phenyl, napthyl, furonyl, thiophenyl, substituted quinolinyl The present invention related to compounds of general FormulaA. The invention provides the synthesis of 2-pyridones useful as potential cardio tonic agents and a process for the preparation thereof.

专利号:US-5736123-A
优先权日:1990-08-09
标 题 :Cocaine receptor binding ligands
发明人：CARROLL FRANK I
权利人:RES TRIANGLE INST
摘要:Novel compounds useful as intermediates in the synthesis of compounds having high affinity for specific cocaine receptors in the brain have the formula ##STR1## wherein R is (CH 2 ) n CH 2 Y, and wherein Y is H or F, X is a pharmaceutically acceptable anion, and n wherein Sn (R 1 , R 2 , R 3 ) is ortho, meta or para and wherein R 1 , R 2 , R 3 are independently alkyl of 1-6 carbon atoms and n is an integer of 0-5.

专利号:EP-3210987-A1
优先权日:2007-08-06
标 题:Process for the synthesis of proteasome inhibitors