A synthetic method was evaluated to form 1 H -isochromeno[3,4- d ]imidazol-5-ones via ring closure starting from 3-amino-4-(arylamino)-1 H -isochromen-1-ones. The method was implemented and optimized in a microreactor environment. It was possible to synthesize these compounds in a continuous mode with an output up to 2.2 g/h.
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Acke et al. (2008) studied this question.
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