Neue Triazenderivate

摘要

1282757 Triazene derivatives FARBENFABRIKEN BAYER AG 25 July 1969 [3 Aug 1968] 37614/69 Heading C2C Novel triazene derivatives of the general formula wherein R1, R2, R3, R4 and R5 are each a hydrogen or halogen atom or an alkyl, alkoxy, alkylthio, alkylsulphinyl or alkylsulphonyl group which may be substituted, or a nitro, cyano, -O(CH 2 ) n -COOY, -(CH 2 ) n COOY, -O(CH 2 ) n -CON(R1) 2 or -(CH 2 ) n CON(R1) 2 group (in which Y is a hydrogen atom or an optionally substituted alkyl group, or a cation such that the salt is pharmaceutically acceptable, n is 0 or an integer from 1 to 5 and R1 is an aliphatic (two aliphatic R1 groups together optionally completing a heterocyclic ring system) or cyclo-aliphatic radical; an SO 3 Y1 or -O(CH 2 ) m N(R11) 2 group (in which Y1 is a hydrogen atom or a cation such that the salt is pharmaceutically acceptable, m is 2, 3 or 4 and R11 is a C 1-4 aliphatic radical) or an esterified carboxy (other than COOY), esterified sulpho, sulphamoyl, N - alkylsulphamoyl, N,N - dialkylsulphamoyl (the two alkyl groups optionally together completing a heterocyclic ring) or acyl group; R1 also possibly being a group of the formula -N=N-NR6R7 in the p-position with respect to X; R6 and R7 are each an alkyl or alkenyl group optionally substituted by a halogen atom; and X is a direct bond, an oxygen or sulphur atom, a carbonyl, sulphonyl sulphoxide, or azo group, an optionally substituted methylene, ethylene or vinylene group, or an ethynylene group; and pharmaceutically acceptable acid addition salts of those derivatives having basic groups are prepared by diazotization of an amine of the general formula and reaction of the product with a secondary amine of the general formula R6R7NH, followed optionally by salification of the product. Pharmaceutical compositions having a selective cell-damaging effect against malignant tumour cells comprise, as active ingredient, at least one triazine derivative of the first general formula above or acid addition salt as defined above, in admixture with a pharmaceutically acceptable diluent or carrier, and may be administered orally, parenterally or rectally.