反应详情

1N Sodium hydroxide (2 mL, 2 mmol) was added to a solution of 3-[5-(2-chlorophenyl)-[1,3,4]oxadiazole-2-yl]-benzoic acid methyl ester (113 mg, 0.36 mmol) in methanol (5 mL) and THF (2 mL), and the reaction mixture stirred at room temperature for 2 h, before neutralizing to pH 7 with 1N hydrochloric acid. The solution was concentrated to dryness in vacuo and placed under high vacuum overnight. Crude material was used directly without purification [MS(Ion spray): 301 and 303 (M++1); LC/MS purity>95%, only major impurity is sodium chloride]. 2-(1H-Benzotriazol-1-yl) -1,1,3,3-tetramethyluronium tetrafluoroborate (TBTU) (116 mg, 0.36 mmol) was added to a room temperature solution/suspension of crude 3-[5-(2-chlorophenyl)-[1,3,4]oxadiazole-2-yl]-benzoic acid and diisopropylethylamine (150 mg, 1.14 mmol) in dimethylfornamide (2 mL), under nitrogen. The reaction mixture was stirred for 10 minutes at room temperature before adding a solution of 4-[3-(N,N-di-tert -butoxycarbonylaminomethyl)phenyl]piperidine (78 mg, 0.2 mmol) and diisopropylethylamine (150 mg, 1.14 mmol) in dimethylformamide (2 mL). The reaction mixture was stirred at room temperature for 16 hours, concentrated to dryness in vacuo, and subjected to dry flash column chromatography on silica with 50:50, dichloromethane:ethyl acetate. 1-{4-[3-(N,N-di-tert -butoxycarbonylaminomethyl)phenyl]-piperidin-1-yl}-1-{3-[5-(2-chloro-phenyl)-[1,3,4]oxadiazole-2-yl]-phenyl}-methanone was isolated as a colorless oil, which was dissolved in dichloromethane (10 mL), cooled at 0° C., and treated with trifluoroacetic acid (1 mL). The reaction mixture was stirred at room temperature under nitrogen for 2 hours, and concentrated to dryness in vacuo. The residue was dissolved in 20% acetonitrile/water [containing 0.1% trifluoroacetic acid] (9 mL) and purified by preparative reverse-phase HPLC (C-18, 10 micron reverse-phase column), eluting with 20% to 60% acetonitrile/water (containing 0.1% trifluoroacetic acid). The product fractions were combined and concentrated to dryness in vacuo. The title compound was isolated as an amorphous white glass solid (98 mg, 83%). 1H NMR [(CD3)2SO]: δ 8.16 (br s, 3H, NH3+) overlapped with 8.22-8.16 (m, 2H) and 8.13 (s, H); 7.79-7.72 (m, 3H); 7.69 (td, H); 7.62 (td, H); 7.41 (s, H); 7.39-7.27 (m, 3H); 4.64 (br d, H); 4.03 (q, 2H); 3.79-3.63 (m, H); 3.28-3.20 (m, H); 3.03-2.80 (m, 2H); 1.96-1.57 (m, 4H). MS(Ion spray): 473 and 475 (M++1).

1. concentrationThe solution was concentrated to dryness in vacuo
2. customplaced under high vacuum overnight
3. customCrude material was used directly without purification [MS(Ion spray): 301 and 303 (M++1)
4. stirringThe reaction mixture was stirred for 10 minutes at room temperature
5. stirringThe reaction mixture was stirred at room temperature for 16 hours
6. concentrationconcentrated to dryness in vacuo
7. dry with materialto dry flash column chromatography on silica with 50:50, dichloromethane