Microwave-Mediated Heterocyclization to Benzimidazo[2,1-b]quinazolin-12(5H)-ones
摘要:
An effective route to benzimidazo[2,1-b]quinazolin-12(5H)-ones from commercially available o-aryl isothiocyanate esters and o-phenylenediamines is reported. This method accommodates a variety of substituents on either starting material and proceeds under microwave irradiation in the presence of barium hydroxide, conditions that do not hydrolyze methyl ester substituents. The pharmacologically pertinent benzimidazoquinazolinone heterocycle is delivered in excellent yield and purity via both solution- and solid-phase protocols, the latter involving traceless release from the resin.
Copper-Catalyzed Domino Synthesis of Benzimidazo[2,1-b]quin- azolin-12(6H)-ones Using Cyanamide as a Building Block
作者:Daoshan Yang、Yuyuan Wang、Haijun Yang、Tao Liu、Hua Fu
DOI:10.1002/adsc.201100580
日期:2012.2
A convenient copper-catalyzeddomino method for the synthesis of benzimidazo[2,1-b]quinazolin-12(6H)-ones has been developed via reactions of readily available substituted 2-bromo-N-(2-halophenyl)benzamides with cyanamide, in which cyanamide acts as a useful buildingblock.
通过容易获得的取代的2-溴-N-(2-卤代苯基)苯甲酰胺与苯的反应,开发了一种方便的铜催化多米诺骨牌合成苯并咪唑并[2,1 - b ]喹唑啉-12(6 H)-酮的方法。氰酰胺,其中氰酰胺可作为有用的结构单元。
Divergent Approach for Regioselective Synthesis of Linearly and Angularly Fused Benzoimidazoquinazolinones from Isatoic Anhydrides
regioselective syntheses of a wide range of linearly and angularly fused benzoimidazoquinazolinones. The selectivity of the products relies on the generation of either highly electrophilic oxyphosphonium or less reactive imidate intermediates. A direct amine attack at the C-2 position of the oxyphosphonium intermediate presumably drives the reaction toward the linearly fused products, whereas an attack of
A synthesis of the quinazolin-4-one pharmacological agent methaqualone from N-(2-carboxyphenyl)oxalamide was developed. A new method for the reductive cyclization of 3-(2-nitrophenyl)quinazolin-4-ones to benzimidazo[2,1-b]quinazolin-12(6H)-ones, the 6-deoxo-6-aza analogs of natural alkaloid tryptanthrine, was suggested and new derivatives of poorly available quinoxalinoquinazolinone fused system were
开发了以N- (2-羧基苯基)草酰胺为原料合成喹唑啉-4-酮药物甲喹酮的方法。 3-(2-硝基苯基)喹唑啉-4-酮还原环化为天然产物6-脱氧-6-氮杂类似物苯并咪唑[2,1 -b ]喹唑啉-12(6 H )-酮的新方法提出了生物碱色胺酮,并合成了难以利用的喹喔啉喹唑啉酮稠合系统的新衍生物。
MATERIALS FOR ELECTRONIC DEVICES
申请人:Stoessel Philipp
公开号:US20130092922A1
公开(公告)日:2013-04-18
The present invention relates to an electronic device comprising anode, cathode and at least one organic layer which comprises a compound of the formula (I) to (IV). The invention furthermore encompasses the use of compounds of the formula (I) to (IV) in an electronic device and to a compound of the formula (Ic) to (IVc).