RESUMO
α-Branched heteroaryl amines are prevalent motifs in drugs and are typically prepared through C-N bond formation. In contrast, C-C bond-forming approaches to branched amines may dramatically expand available chemical space but are rarely pursued in parallel format due to a lack of established library protocols. Methods for the synthesis of α-branched heteroaryl amines via aldimine addition have been evaluated for compatibility with parallel synthesis. In situ activation of aliphatic carboxylic acids as redox-active esters enables Zn-mediated decarboxylative radical imine addition to access aliphatic-branched heterobenzylic amines. In situ activation of (hetero)aryl bromides via Li-halogen exchange enables heteroaryl-lithium addition to imines to access (hetero)benzhydryl amines. Condensation of heteroaryl amines with heteroaryl aldehydes provides aldimines which may be intercepted with aryl Grignard reagents to provide modular access to (hetero)benzhydryl amines. These protocols minimize synthetic step count and maximize accessible design space, enhancing access to α-branched heteroaryl amines for medicinal chemistry.
Assuntos
Aminas , Química Farmacêutica , Aldeídos/química , Aminas/química , Ácidos Carboxílicos , Iminas/químicaRESUMO
It is found that in a buffer solution of HAc-NaAc (pH-6.0), iron (III) and aluminium (III) react with ethylene glycol diethy diaminoteracetic acid (EGTA), pyrogallol red (PR) and cetylpyridinium bromide (CPB) to form quarternary complex. Micro iron (III) and aluminium (III) can be simultaneous determined by the first derivative spectrophotometry of the quarternary complex. The RSD for the determinations of iron and aluminium are 4.5% and 1.1% respectively, and the recoveries are 93%-98% and 95%-102% respectively. This method has been applied to the determination of micro iron and aluminum in quartz sand with satisfactory results.