[Synthetic studies of substituted quinazolinone].

Y Eguchi, A Sugimoto, M Ishikawa
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Abstract

We re-examined 2-methyl-3-(2-chlorophenyl)-6-ethoxycarbonyl-5,7-dimethyl-4 (3H)-quinazolinone to be hydroxymethylated by means of selenium oxide oxidation, followed by Ca (BH4)2 reduction. Chlorination reaction of 2-hydroxymethyl quinazolinone proceeded effectively by use of PCl5 in anhyd. benzene at room temperature. Thus, we prepared new compounds in respect of substituted quinazolinone.

取代喹唑啉酮的合成研究。
我们重新研究了2-甲基-3-(2-氯苯基)-6-乙氧羰基-5,7-二甲基-4 (3H)-喹唑啉酮在氧化硒氧化下的羟甲基化,然后再进行Ca (BH4)2还原。在酸酐中使用PCl5进行2-羟甲基喹唑啉酮的氯化反应有效。室温下的苯。因此,我们在取代喹唑啉酮方面制备了新的化合物。
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