55. Synthesis of 10-(3′-methanesulfonamidopropyl)-1,ALK activation 8-diazaphenothiazine (23) To a stirred solution of oil with 10-aminopropyl-1,8-diazaphenothiazine (21) (0.129 g, 0.5 mmol) in a mixture of CH2Cl2 (5 ml) and 10 % aqueous Na2CO3 solution (5 ml) a solution of methanesulfonyl chloride (0.12 ml, 1.5 mmol) in CH2Cl2 (3 ml) was added. The solutions were stirred at rt for 24 h. The organic phase was separated and aqueous phase was extracted with CH2Cl2 (2 × 5 ml). The combined extracts were
washed with water (10 ml) and dried with anhydrous sodium sulfate and evaporated in vacuo. The residue was purified by column chromatography (aluminum oxide, CH2Cl2) to give 0.125 g (74 %) 10-(3′-methanesulfonamidopropyl-1,8-diazaphenothiazine (23) as an oil. 1H NMR (CDCl3) δ 2.08 (m, 2H, CH2), 2.94 (s, 3H, CH3), 3.42 (m, 2H, NCH2), 4.02 Selleckchem GW572016 (t, J = 6.9 Hz, 2H, NCH2), 5.57 (broad s, 1H, NH), 6.74 (dd, J = 7.2 Hz, J = 5.0 Hz, 1H, H3), 6.84 (d, J = 5.0 Hz, 1H, H6), 7.14 (dd, J = 7.2 Hz, J = 1.4 Hz 1H, H4), 7.97 (dd, J = 5.0 Hz, J = 1.4 Hz 1H, H2), 8.03
(d, J = 5.0 Hz, 1H, H7), 8.18 (s, 1H, H9). FAB MS m/z: 337 (M+1, 100), 202 (M+1-C3H5NHSO2CH3,30). Anal. calcd. For C14H16N4O2S2: C 49.98; H 4.79; N 16.65. Found: C 49.88; H 4.74; N 16.39. Synthesis of 10-(3′-chloroethylureidopropyl)-1,8-diazaphenothiazine AR-13324 cell line (24) To a stirred solution of 10-aminopropyl-1,8-diazaphenothiazine (21) (0.129 g, 0.5 mmol) in dry EtOH (10 ml) at 0 °C 2-chloroethyl isocyanate (0.87 ml, 1 mmol) was added. The mixture
was stirred at 0 °C for 0.5 h and at rt for 24 h. After evaporation of EtOH in vacuo the residue was purified by column chromatography (aluminum oxide, CH2Cl2) to give 0.120 g (63 %) 10-chloroethylureidopropyl-1,8-diazaphenothiazine (24), mp 103 °C. 1H NMR (CDCl3) δ 1.75 (m, 2H, CH2), 2.10 (m, 2H, CH2), 3.49 (m, 4H, 2CH2), 4.46 (m, 2H, CH2), 6.76 3-oxoacyl-(acyl-carrier-protein) reductase (dd, J = 7.2 Hz, J = 5.1 Hz, 1H, H3), 6.84 (d, J = 5.0 Hz, 1H, H6), 7.14 (dd, J = 7.2 Hz, J = 1.4 Hz 1H, H4), 7.96 (dd, J = 5.1 Hz, J = 1.4 Hz 1H, H2), 8.01 (d, J = 5.0 Hz, 1H, H7), 8.17 (s, 1H, H9). FAB MS m/z: 364 (M+1, 30), 202 (M+H-C3H6NHCONHCH2CH2Cl, 10), 185 (2gly + H, 100). Anal. calcd. for C16H18ClN5OS: C 52.82, H 4.99, N 19.25. Found: C 52.77; H 4.97; N 19.11. Biological assays Preparation of the compounds for biological assays The compounds were dissolved in DMSO (10 mg/ml) and subsequently diluted in RPMI-1640 cell culture medium (see below). Isolation of the peripheral blood mononuclear cells Venous blood from a single donor was withdrawn into heparinized syringes and diluted twice with phosphate-buffered saline.