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General Procedure for the Synthesis of (S)-11, Butylamino)-2,3-dihydro-1H-benzo[e]pyrrolo[1, 2-a][1,4]-diazepin-5-(11aH)-one (5a) Method A Thiolactam (4, 0.232 g, 1 mmol) was suspended in n-BuNH2 (4 mL) and heated to 60°C. At this temperature HgCl2 (0.272 g, 1 mmol) was added, and the mixture was heated over a period of 1 h at reflux temperature. After cooling, the reaction mixture was filtered through a plug of Celite and washed with CHCl3. The filtrate was washed with aq Na 2S2O3 and dried over Na2SO 4. The solvent and excess amine were distilled off in vacuo. The residue was then chromatographed (SiO2, PE-EtOAc, 1:5, Method B Bi(NO3)3 (0.395 g, 1 mmol) was used. Method C Compound 1 (0.190 g, 1 mmol) was used and heated as described. Then, the re
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3O: C, 70.82; H, 7.80; N, 15.49. Found: C,70.58; H, 7.41; N, 14.91.
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