Abstract
1,4-Dihydro-quinazoline-4-on-1-yl-acetic acids5 were prepared by reaction of 3,1-benzoxazine-2,4-diones1 with ammonia to2. Cyclisation of2 gave4 and their hydrolysis lead to5. 2-Substituted quinazolinones9 could be obtained by reaction of2 with acid chlorides or by reaction of1 with amidines. Quinazolinone8 was synthesized in a similar way. The substituted 2-aminobenzamide10 showed a reaction behaviour different from that of2.
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Literatur
Schmidt J., Süsse M., Johne S., Org. Mass Spectrom.20, 184 (1985) (4. Mitt.).
Süsse M., Johne S., J. prakt. Chem.326, 1027 (1984).
Johne S., Fortschr. Arzneimittelforschung26, 259 (1982).
Süsse M., Johne S., Z. Chem.21, 431 (1981).
Ziegler E., Steiger W., Kappe Th., Monatsh. Chem.100, 948 (1969).
Naik N. R., Amin A. F., Patel S. R. J. Indian Chem. Soc.56, 708 (1979).
Ozaki K., Yamada Y., Oine T., Chem. Pharm. Bull.31, 2234 (1983).
Ozaki K., Yamada Y., Oine T., Chem. Pharm. Bull.28, 702 (1980).
Oine T.,Yamada Y.,Ozaki K.,Wakamoto S., Jap. Pat. Kokai 77-153983 (1977); Chem. Abstr.88, 190882 (1978).
Oine T.,Ozaki K.,Yamada Y., Jpn. Kokai Tokkyo Koho 7909, 290; Chem. Abstr.91, 39517c (1979).
Ozaki K., Yamada Y., Oine T., J. Org. Chem.46, 1571 (1981).
Süsse M.,Johne S.,Herzberg B.,Schaks A., DDR-WP C 07 D 2401067 (1982).
Miki T.,Asano M., EPÜ-Patent 9608; C 07 C 103/50.
Süsse M., Johne S., J. prakt. Chem.326, 342 (1984).
Süsse M.,Johne S., DDR-Pat. 222 307 (1983).
Süsse M.,Johne S., DDR-Pat. 221 737 (1983).
Hartmann G. E., Koletar G., Pfister D. R., J. Heterocycl. Chem.12, 565 (1975).
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Dem Andenken von Dr.Wolfgang Truppe († 24. 11. 1984) gewidmet.
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Süsse, M., Johne, S. Chinazolincarbonsäuren, 5. Mitt.: Synthese von 1,4-Dihydro-chinazolin-4-on-1-yl-essigsäuren und Estern. Monatsh Chem 117, 499–509 (1986). https://doi.org/10.1007/BF00810899
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DOI: https://doi.org/10.1007/BF00810899