Hydrazine → 2-(3-Piperidinomethylthiophenoxy)ethylamine
反応式
NN.Br.[N:4]1([CH2:10][C:11]2[CH:12]=[C:13]([CH:28]=[CH:29][CH:30]=2)[S:14][CH2:15][CH2:16][N:17]2C(=O)C3=CC=CC=C3C2=O)[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1>C(O)C>[N:4]1([CH2:10][C:11]2[CH:12]=[C:13]([CH:28]=[CH:29][CH:30]=2)[S:14][CH2:15][CH2:16][NH2:17])[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5]1参加物
4
実験手順
Anhydrous hydrazine (1.79 g, 56.0 mmoles) was added to a suspension of N-{2-[3-(piperidinomethyl)thiophenoxy]ethyl}phthalimide hydrobromide (5.17 g, 11.2 mmoles) [prepared in Step D] in 200 mL of 95% ethanol, stirred at ambient temperature for 18 hours and filtered. The filtrate was stripped and the semi-solid residue was stirred with several portions of ether. Evaporation of the solvent gave 2.8 g of title compound as a yellow oil.