(fused) benz(thio)amides

C - Chemistry – Metallurgy – 07 – D

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C07D 405/04 (2006.01) C07D 215/48 (2006.01) C07D 257/04 (2006.01) C07D 311/24 (2006.01) C07D 319/20 (2006.01) C07D 401/04 (2006.01) C07D 409/04 (2006.01) C07D 409/12 (2006.01) C07D 409/14 (2006.01) C07D 413/04 (2006.01)

Patent

CA 1261835

0-01-38526C/JK/85 TITLE OF THE INVENTION (FUSED) B E N Z (THIO) A M I D E S A B S T R A C T A novel (fused) benz(thio)amides of the general formula: Image (I) (wherein, symbol A represents a single bond or a group of methylene, ethylene, trimethylene, tetramethylene, vinylene, propenylene, butenylene, butadienylene or ethynylene group optionally being substituted by one, two or three of straight or branched alkyl group(s) of from 1 to 10 carbon atom(s) and/or phenyl group(s). Symbol B represents (i) a carbocyclic ring of from 4 to 8 members being unreplaced or replaced one, two or three of optional carbon atom(s) by oxygen, nitrogen and/or sulphur atom(s). (The ring may optionally be substituted by group(s) of oxo, thioxo and/or hydroxy group(s).) or (ii) a divalent group of formula: - A-1 - Image or Image Symbol T represents an oxygen atom or a sulphur atom. R1 represents a group of general formula: (i) Image (ii) Image or (iii) Image or (iv) a straight or branched alkyl, alkenyl or alkynyl group or from 1 to 20 carbon atom(s). (wherein R5 and R6 independently represent a hydrogen atom or a halogen atom or a straight or branched alkyl, alkenyl or alkynyl group of from 1 to 20 carbon atom(s) being unreplaced or replaced one, two,three, four or five of optional carbon atom(s) by oxygen atom(s), sulphur atom(s), halogen atom(s), nitrogen atom(s), benzene ring(s), thiophene ring(s), naphthalene ring(s), carbocyclic ring(s) or from 4 to 7 carbon atom(s), carbonyl group(s), carbonyloxy group(s), hydroxy - A-2 - group(s), carboxy group(s), azido group(s) and/or nitro croup(s)). R2 represents a hydrogen atom or a straight or branched alkyl group of from 1 to 6 carbon atom(s) R3 represents a hydrogen atom, a halogen atom, a hydroxy group, a nitro group, a group of general formula: -COOR7 (wherein R7 represents a hydrogen atom or a straight or branched alkyl group of from 1 to 6 carbon atom(s).) or a straight or branched alkyl, alkoxy or alkylthio group of from 1 to 6 carbon atom(s). R represents (i) when symbol B represents a closed ring, a group of general formula: Image Image or Image Image (wherein symbol U represents an oxygen atom or a sulphur atom. R8 represents a hydrogen atom or a straight or branched alkyl group of from 1 to 6 carbon atom(s). n and m represent an integer of from 1 to 10, respectively, p and q represent zero or an integer of from 1 to 10, respectively.) or - A-3 - (ii) when symbol B do not represent a ring, a group of general formula: Image or Image (wherein R8, p and q represent the same meaning as depicted hereinbefore. With the proviso that, when the symbol B represents a group of formula: Image p does not represent zero.) With the proviso that, following compounds are excluded, i.e. compounds of general formula: Image (I') (wherein the symbol A' is 2 vinylene or ethylene group optionally being substituted by straight or branched alkyl group(s) of from 1 to 4 carbon atom(s), R4' is the general formula: -(CH2)n-COOR8 (wherein all the symbols axe the same meaning as depicted hereinbefore.) and R1' is (i) a group of the general formula: - A-4 - Image (wherein R5' and R6' are hydrogen atom(s), hydroxy group(s), halogen atom(s), straight or branched alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy, alkynyloxy or acyloxy group(s) of from 1 to 4 carbon atom(s) or cycloalkyl group(s) of from 3 to 6 carbon atom(s), independently.) or (ii) a group of the general formula: Image (wherein R5' and R6' are the same meaning as depicted hereinbefore.)) or non-toxic salts thereof possess an antagonistic activity on leukotrienes (SRS), inhibitory activity on 5.alpha.-reductase, on phosphtolipase and on aldose reductase and are therefore useful for the prevention and/or treatment for diseases induced by leukotrienes, 5.alpha.-reductase, phospholipase and aldose reductase in mammals, especially human beings. - A-5 -

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