Summary
Quinaozolin-2,4-(1H,3H)-dione (1), 6,7-dimethoxy-quinazolin-2,4-(1H,3H)-dione (2), and 1,2,3,4-tetrahydro-2,4-dioxo-pyrido[2,3-d]pyrimidine (3) were subjected to Mitsunobu conditions using propinol to give the 1,3-dialkylated derivatives4,5, and6.
Zusammenfassung
Chinazolin-2,4-(1H,3H)-dion (1), 6,7-Dimethoxychinazolin-2,4-(1H,3H)-dion (2) und 1,2,3,4-Tetrahydro-2,4-dioxo-pyrido[2,3-d]pyrimidin (3) werden unter Mitsunobu-Bedingungen mit Propinol umgesetzt und ergeben die 1,3-dialkylierten Derivate4,5 und6.
References
Acetylenic Chemistry, XXV: Reisch J., Iding M., Schönweiler D. (in press) J. Heterocycl. Chem.
Reisch J., Usifoh C. O., Oluwadiya J. O. (1992) Monatsh. Chem.123: 247
Reisch J., Usifoh C. O., Oluwadiya J. O. (1990) J. Heterocycl. Chem.27: 1953
Reisch J., Usifoh C. O., Okoh E., Oluwadiya J. O., (1992) Pharmazie47: 18
Amiss A. M., Mehta D. R., Samarth S. S. (1970) Prog. Drug Res.14: 218
Akgiin H., Hollstein U., Hurwitz L. (1988) J. Pharm. Sci.77: 735
Johne S. (1982) Prog. Drug Res.26: 259
Vida J. A. (1977) Anticonvulsants. Academic Press, New York, pp. 428, 432–450, 471–472
Sent to National Cancer Institute (NCI), Bethesda, Maryland, USA, for anti-cancer screening
Danielsson B., Skoglund E. (1965) Acta Pharm. Suec.2: 167
Reisch J., Usifoh C. O., Oluwadiya J. O. (1990) J. Heterocycl. Chem.27: 287
Mitsunobu O. (1981) Synthesis: 1
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Reisch, J., Rao, A.R.R. & Usifoh, C.O. Acetylenic chemistry, part XXVI: One-pot synthesis of 1,3-dialkylated derivatives of quinazolinone and its aza-analogue via mitsunobu reaction. Monatsh Chem 124, 1217–1220 (1993). https://doi.org/10.1007/BF00810032
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DOI: https://doi.org/10.1007/BF00810032