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C(3)-alkylation and cyclization of pyrazino[1,2-b]isoquinolin-4-ones

机译:吡嗪并[1,2-b]异喹啉-4-酮的C(3)-烷基化和环化

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摘要

To avoid the epimerization of the C(11a)-stereocenter previously observed in 6,11a-cis-pyrazino[1,2-b]isoquinolin-1,4-diones, we present in this paper the C(3)-alkylation of 1-methoxy-pyrazino[1,2-b]isoquinolin-4-ones to obtain all-cis derivatives through a very reliable protocol. The success of the acid-promoted cyclization to get pentacyclic (R-3=arylmethyl) or tetracyclic (R-3=2-bromo-2-propenyl) compounds is dependent on the nature of the C(3)-unsaturated chain and of the N-substituent, but these limitations have been overcome by using trifluoromethanesulfonic as a superacid catalyst. The C-(3)-alkylation of pyrazinol 1,2-b]isoquinolin-4-one is also Studied.
机译:为避免先前在6,11a-顺式吡嗪并[1,2-b]异喹啉-1,4-二酮中观察到的C(11a)-立体中心差向异构化,我们在本文中提出了C(3)-烷基化1-甲氧基-吡嗪并[1,2-b]异喹啉-4-酮通过非常可靠的方案获得全顺式衍生物。酸促进环化获得五环(R-3 =芳基甲基)或四环(R-3 = 2-溴-2-丙烯基)化合物的成功取决于C(3)-不饱和链的性质和N-取代基,但通过使用三氟甲磺酸作为超强酸催化剂克服了这些限制。还研究了吡嗪醇1,2-b]异喹啉-4-酮的C-(3)-烷基化。

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