Araliphatic dihalogen compounds and process for their...

C - Chemistry – Metallurgy – 07 – C

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C07C 31/00 (2006.01) C07C 29/147 (2006.01) C07C 29/60 (2006.01) C07C 43/295 (2006.01) C07C 57/58 (2006.01) C07C 57/60 (2006.01) C07C 57/76 (2006.01) C07C 59/56 (2006.01) C07C 59/68 (2006.01) C07C 69/76 (2006.01) C07F 1/00 (2006.01) C07F 9/40 (2006.01)

Patent

CA 1086770

ABSTRACT OF THE DISCLOSURE Compounds of the formula Image wherein R1 and R2 are the same or different and are F, Cl or Br; Q is -CH(CH3)-CH2-, -C(OH)(CH3)-CH2- or -C(CH3)=CH-; Y is COOH, COOR3, CH2OH or CH2OAc; n is 0 or 1; R3 is alkyl, aryl of up to 8 carbon atoms or C6H4NHCOCH3; and Ac is alkanoyl of 1 - 8 carbon atoms; and physiologi- cally acceptable salts thereof, are anti-inflammatory agents. Such com- pounds can be made from compounds of the formula Z - X, wherein Z is Image , wherein X is CE(CH3)-CH2Y, CE(CH3)-CH[P=O(OR4)2], -CH(CH3)-C(=PAr3)-Y, CH(CH3)-CH(CO-R4)-Y or -QW wherein E is Hal, Hal being Cl, Br or I, or a functionally-modified hydroxyl group selected from an alcoholate and an acylate, R4 is alkyl of 1 - 12 carbon atoms, aryl of 6 - 12 carbon atoms, or aralkyl of 7 - 12 carbon atoms, and W is functionally-modified COOH group selected from an ester, a nitrile, an iminoether and an amide, or a functionally-modified CH2OH selected from an alcoholate and an acylate which differs from Y, and R1, R2, n, Y, and Q are as defined above, and X can thus be converted to -Q-Y, where Q and Y are as defined above. The compounds also have analgesic and antipyretic effects, lowering of the liquid level, i.e., chlolesterol and triglyceride level and inhibiting thrombocyte aggregation.

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