| 摘要 |
1341698 Indenophthalazines ASPRONICHOLAS Ltd 19 April 1971 [14 March 1970] 12424/70 Heading C2C The invention comprises compounds of formula and their acid addition and quaternary ammonium salts, wherein R 1 and R 2 are each H, OH, halogen, CN, NO 2 , NH 2 or C 1-6 alkyl or alkoxy, and R is (i) NR 3 R 4 (but not NH 2 ) where R 3 and R 4 are each H, alkyl, hydroxyalkyl, haloalkyl, substituted Ph, Ph-alkyl, substituted Ph-alkyl, C 3-8 cycloalkyl or (C 3-8 -cycloalkyl)- alkyl, or (ii) (NH-A) n -X, where A is C 1-4 alkylene or the unsaturated analogue, n is 0 or 1 and X is pyrrolidine, piperidine or hexamethyleneimine or their unsaturated analogues, or analogous rings where one C atom is replaced by O, N or S (when n is 0, X must be attached by its N atom to the indenophthalazine ring), or X is 4-substituted piperazino. The term "alkyl" in the foregoing includes the analogous alkenyl and alkynyl radicals. These compounds are prepared by reacting a corresponding 3-haloindenophthalazine (obtained from the indenophthalazone with POCl 3 ) with HR, or by standard interconversion procedures from compounds thus obtained. Also prepared is 3- chlorofluorenone-1-carboxylic acid. Therapeutic compositions for oral, parenteral or rectal administration comprise compounds of the above formula, which have anti-inflammatory (especially antirheumatic) activity, and in some cases immunosuppressive activity. |
