Monoamino 2,4,5-trisubstituted oxazoles

Chemistry of carbon compounds – Miscellaneous organic carbon compounds – C-metal

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424272, 542408, 542418, C07D26334

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active

040726894

ABSTRACT:
Pharmacologically active 2,4,5-trisubstituted oxazoles of the general formula ##STR1## wherein A is cyclohexyl, thienyl or a group of the formula ##STR2## in which R represents one to three substituents each independently selected from the group consisting of hydrogen, lower alkyl, halo, halo-lower alkyl, lower alkoxy, nitro, cyano, amino, carbamoyl, acetamino or carboxy; one of the R.sub.1 and R.sub.2 groups is a lower alkyl group and the other is an amido group, ##STR3## wherein R.sub.3 is selected from the group consisting of hydrogen, lower alkyl, lower alkenyl, cycloalkyl, phenyl, substituted phenyl, phenyl-lower alkyl, hydroxy-lower alkyl, lower acyloxy-lower alkyl, hydroxy, amino, lower alkylideneamino, cycloalkylideneamino, benzylideneamino and R.sub.4 is selected from hydrogen, lower alkyl, lower alkenyl, cycloalkyl, phenyl, substituted phenyl, phenyl-lower alkyl, hydroxy-lower alkyl, lower acyloxy-lower alkyl, or R.sub.3 and R.sub.4 taken together with the nitrogen atom may also form a 5- to 7-membered hetero ring which may contain one other hetero atom selected from N, O and S. The compounds have antiinflammatory activity.

REFERENCES:
"Beilsteins Handbuch der Org. Chemie.," Band XXVII, Syst. #4309, p. 324, (1937).
Zerilli et al., "Chem. Abst.," vol. 78, (1973), Abst. No. 92286j.
Sycheva et al., "Chem. Abst.," vol. 58, (1962), p. 1443h.
Finar, "Organic Chem.," vol. 1, p. 189, (1959), 3rd Ed.

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