(3S)-3-tert-butylpiperazine-2,5-dione

反応条件: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

実験手順: Lithium aluminum hydride(1 M solution in THF, 40 mL, 40.0 mmol) was added drop wise to solution of (S)-2-tert-butylpiperazin-3,6-dione (1.5 g, 8.82 mmol) in THF (50 mL) at 0° C. The reaction mixture was stirred at room temperature for 7 days and at 65° C. for 17 h, then cooled to 0° C. and quenched sequentially with H2O (1.7 mL), 10% NaOH (2.2 mL) and H2O (3.4 mL). Ether (100 mL) was added to the reaction mixture, and stirring was continued for 1.5 h. The solid was filtered, the filtrate was concentrated and purified by column chromatography (silica gel, 33% EtOAc in hexanes) to afford (S)-2-tert-butylpiperazine (0.64 g, 52%) as a clear oil. 1H NMR and MS consistent. cooled to 0° C. quenched sequentially with H2O (1.7 mL), 10% NaOH (2.2 mL) and H2O (3.4 mL) Ether (100 mL) was added to the reaction mixture stirring was continued for 1.5 h The solid was filtered the filtrate was concentrated purified by column chromatography (silica gel, 33% EtOAc in hexanes)

反応条件: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

実験手順: Lithium aluminum hydride(1 M solution in THF, 40 mL, 40.0 mmol) was added drop wise to solution of (S)-2-tert-butylpiperazin-3,6-dione (1.5 g, 8.82 mmol) in THF (50 mL) at 0° C. The reaction mixture was stirred at room temperature for 7 days and at 65° C. for 17 h, then cooled to 0° C. and quenched sequentially with H2O (1.7 mL), 10% NaOH (2.2 mL) and H2O (3.4 mL). Ether (100 mL) was added to the reaction mixture, and stirring was continued for 1.5 h. The solid was filtered, the filtrate was concentrated and purified by column chromatography (silica gel, 33% EtOAc in hexanes) to afford (S)-2-tert-butylpiperazine (0.64 g, 52%) as a clear oil. 1H NMR and MS consistent. cooled to 0° C. quenched sequentially with H2O (1.7 mL), 10% NaOH (2.2 mL) and H2O (3.4 mL) Ether (100 mL) was added to the reaction mixture stirring was continued for 1.5 h The solid was filtered the filtrate was concentrated purified by column chromatography (silica gel, 33% EtOAc in hexanes)

反応条件: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

実験手順: Lithium aluminum hydride(1 M solution in THF, 40 mL, 40.0 mmol) was added drop wise to solution of (S)-2-tert-butylpiperazin-3,6-dione (1.5 g, 8.82 mmol) in THF (50 mL) at 0° C. The reaction mixture was stirred at room temperature for 7 days and at 65° C. for 17 h, then cooled to 0° C. and quenched sequentially with H2O (1.7 mL), 10% NaOH (2.2 mL) and H2O (3.4 mL). Ether (100 mL) was added to the reaction mixture, and stirring was continued for 1.5 h. The solid was filtered, the filtrate was concentrated and purified by column chromatography (silica gel, 33% EtOAc in hexanes) to afford (S)-2-tert-butylpiperazine (0.64 g, 52%) as a clear oil. 1H NMR and MS consistent. cooled to 0° C. quenched sequentially with H2O (1.7 mL), 10% NaOH (2.2 mL) and H2O (3.4 mL) Ether (100 mL) was added to the reaction mixture stirring was continued for 1.5 h The solid was filtered the filtrate was concentrated purified by column chromatography (silica gel, 33% EtOAc in hexanes)

反応条件: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

実験手順: Lithium aluminum hydride(1 M solution in THF, 40 mL, 40.0 mmol) was added drop wise to solution of (S)-2-tert-butylpiperazin-3,6-dione (1.5 g, 8.82 mmol) in THF (50 mL) at 0° C. The reaction mixture was stirred at room temperature for 7 days and at 65° C. for 17 h, then cooled to 0° C. and quenched sequentially with H2O (1.7 mL), 10% NaOH (2.2 mL) and H2O (3.4 mL). Ether (100 mL) was added to the reaction mixture, and stirring was continued for 1.5 h. The solid was filtered, the filtrate was concentrated and purified by column chromatography (silica gel, 33% EtOAc in hexanes) to afford (S)-2-tert-butylpiperazine (0.64 g, 52%) as a clear oil. 1H NMR and MS consistent. cooled to 0° C. quenched sequentially with H2O (1.7 mL), 10% NaOH (2.2 mL) and H2O (3.4 mL) Ether (100 mL) was added to the reaction mixture stirring was continued for 1.5 h The solid was filtered the filtrate was concentrated purified by column chromatography (silica gel, 33% EtOAc in hexanes)