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Synthesis of New Derivatives of 4-(4,7,7-Trimethyl-7,8-dihydro-6H-benzo[b]pyrimido[5,4-e][1,4]thiazin-2-yl)morpholine
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Cyclocondensation of het2556-eo-0001">5-amino-6-methyl-2-morpholinopyrimidine-4-thiol (het2556-eo-0001" rel="references:#jhet2556-eo-0001">) and het2556-eo-0002">2-bromo-5,5-dimethylcyclohexane-1,3-dione (het2556-eo-0002" rel="references:#jhet2556-eo-0002">) under mild reaction condition afforded het2556-eo-0003">4,7,7-trimethyl-2-morpholino-7,8-dihydro-5H-benzo[b]pyrimido[5,4-e][1,4]thiazin-9(6H)-one (het2556-eo-0003" rel="references:#jhet2556-eo-0003">). The 1H and 13C NMR data of compound (het2556-eo-0003" rel="references:#jhet2556-eo-0003">) are demonstrated that this compound exists primarily in the enamino ketone form. Reaction of compound (het2556-eo-0003" rel="references:#jhet2556-eo-0003">) with het2556-eo-2004">phosphorous oxychloride gave het2556-eo-0004">4-(9-chloro-4,7,7-trimethyl-7,8-dihydro-6H-benzo[b]pyrimido[5,4-e][1,4]thiazin-2-yl)morpholine (het2556-eo-0004" rel="references:#jhet2556-eo-0004">). Nucleophilic substitution of chlorine atom of compound (het2556-eo-0004" rel="references:#jhet2556-eo-0004">) with typical secondary amines in DMF and K2CO3 furnished the new substituted derivatives of 4-(4,7,7-trimethyl-7,8-dihydro-6H-benzo[b]pyrimido[5,4-e][1,4]thiazin-2-yl)morpholine (het2556-eo-0006" rel="references:#jhet2556-eo-0006 #jhet2556-eo-0007 #jhet2556-eo-0008 #jhet2556-eo-0009 #jhet2556-eo-0010 #jhet2556-eo-0011 #jhet2556-eo-0012 #jhet2556-eo-0013">). All the synthesized products were characterized and confirmed by their spectroscopic and microanalytical data.

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