“…Co-occurrence of both functional groups in one quinoline molecule broaden the above potential, as was shown for 4-chloro-3-quinolinesulfonyl chloride (5b) 4,5 and 2-chloro-6-quinolinesulfonyl chloride (5c) 6 in studies directed at the preparation of biologically active compounds. [1][2][3][4][5][6] The 3-or 7-chlorosulfonyl-4-chloroquinolines (5b,e), 4,5,8 8chlorosulfonyl-4-chloroquinolines, 7 4-chlorosulfonyl-7-chloroquinoline (8e), 8 and 2-chloro-6-quinolinesulfonyl chloride (5c), 6 are well known but only the 4,7-isomers 5e and 8e were prepared from the respective dichloroquinoline (1e). 8 Azinesulfonyl chlorides could be directly obtained by oxidative chlorination of thioazines -thiols 8,9,10 disulfides, 8,9 benzylsulfides 5,11 with a thio substituents at non-aza-activated positions.…”