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Part-IExperimentalperiod of 15-20 min. Reaction was worked up as described for the compound IIIi to getthe title compound.M.P. : 264-266 o C; Yield: 68%.Mol. Formula : C 19 H 18 N 4 OS 2 ; Mol. Wt. 382.5.IR (KBr) cm -1 : 3212(γ NH ), 2916(γ C-H ), 1685(γ CONH ), 737(γ C-S ).NMR (DMSO-d 6 )δppm : 1.68 (6H, m, CH 2 at 6, 7, & 8), 1.88 (2H, t, CH 2 at 5, J = 3.36),3.30 (2H, t, CH 2 at 9, J = 5.36), 4.36 (2H, s, CH 2 at SCH 2 ), 7.20(2H, m, H at imidazole), 7.56 (2H, m, H at imidazole, J =3.16), 12.50 (1H, s, NH), 13.40 (1H, s, NH).MS m/e : 382(M + ), 349, 232, 150.23. Synthesis of 2-{[(5-methoxy-1H-benzimidazol-2-yl)thio]methyl}-3,5,6,7,8,9-hexahydro-4H-cyclohepta[4,5]thieno[2,3-d]pyrimidin-4-one(IIIxxiii)2-Mercapto-5-methoxybenzimidazole (1.8 gm; 0.01 mole) was dissolved in 25 ml of 10%sodium hydroxide solution by stirring at room temperature. To this clear solution pinch ofTEBA chloride was added and stirring was further continued for 10 min. To this wellstirred solution, added clear solution of 2-chloromethyl-3,5,6,7,8,9-hexahydro-10-thia-1,3-diaza-benzo[a]azulen-4-one (IIxii, 2.68 gm; 0.01 mole) in methylene dichloride (25ml), over a period of 15-20 min. Reaction was worked up as described for the compoundIIIi to get the title compound.M.P. : 226-230 o C; Yield: 70%.Mol. Formula : C 20 H 20 N 4 O 2 S 2 ; Mol. Wt. 412.5.IR (KBr) cm -1 : 3190(γ NH ), 2918(γ C-H ), 1685(γ CONH ), 750(γ C-S ).NMR (DMSO-d 6 )δppm : 1.66 (4H, m, CH 2 at 6 & 7), 1.87 (2H, m, CH 2 at 5), 2.85 (2H,m, CH 2 at 8), 3.29(2H, m, CH 2 at 9), 3.84 (3H, s, CH 3 atOCH 2 ), 4.34 (2H, s, SCH 2 ), 6.79-7.43 (3H, m, Ar-H), 12.30(1H, s, NH), 13.21 (1H, s, NH).MS m/e : 412(M + ), 379, 232, 180.24. Synthesis of 2-(1H-benzimidazol-2-yl)methylthioquinazolin-4-(3H)-one (IIIxxiv)2-Mercaptobenzimidazole (1.5 gm; 0.01 mole) was dissolved in 25 ml of 10% sodiumhydroxide solution by stirring at room temperature. To this clear solution pinch of TEBA197