A short synthesis of the parp inhibitor 2-(4-trifluoro-methylphenyl)benzimidazole-4-carboxamide (NU1077)
作者:Steven C. Austen、John M. Kane
DOI:10.1002/jhet.5570380427
日期:2001.7
A four-step synthesis of the PARPinhibitor2-(4-trifluoromethylphenyl)benzimidazole-4-carboxamide (1, NU1077) is presented. Condensation of 2,3-diaminotoluene and 4-trifluoromethylbenzaldehyde afforded 4-methyl-2-(4-trifluoromethylphenyl)benzimidazole. Oxidation of the methyl group with potassium permanganate in warm t-butanol afforded the carboxylic acid that was converted to the corresponding carboxamide
choice for the quinazolines, while the solid-state melt reaction is more efficient for derivatives of (iso)nicotinic based hydrazones. Crystalline amine-functionalised hydrazones 4a and 4b undergo post-synthetic modifications in reactions with 3- or 4-pyridinecarbaldehyde vapours to form hydrazone-Schiff bases 4a-3py, 4b-3py, 4a-4py, and 4b-4py. Mechanochemical and vapour-mediated reactions are followed
A novel 3-D large porous metalâorganic framework was achieved from triple metal helices via
ÏâÏ stacking interactions between the aromatic groups of the helices.
通过三重金属螺旋的芳香基团之间的ÏÏÏ堆叠相互作用,实现了一种新型的三维多孔金属有机框架。
METHOD USING FLUORESCENT TURN-ON PROBES FOR CELL-SPECIFIC DETECTION
申请人:Agency for Science, Technology and Research
公开号:US20150192589A1
公开(公告)日:2015-07-09
The invention provides method for imaging the activity of enzymes or bioactive molecules in cells using fluorescent probes with aggregation-induced emission properties and excited-state intramolecular proton transfer properties. The fluorescent probes prepared according to the invention are those of formula (I),
wherein W, X, Y, Z have the meaning as described in the description, R is a reactive group that can interact with enzymes and other bioactive molecules, Linker is a single bond or a combination of chemical bonds linking the targeting group T to the probe molecule, and T represents a targeting group that has an ability to interact with an organelle.