1-Piperazinecarboxylic acid, ethyl ester → HCID 21423023、化合物

反応式

[CH2:1]([O:3][C:4]([N:6]1[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1)=[O:5])[CH3:2].CS(O[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])(=O)=O.C(=O)([O-])[O-].[Na+].[Na+]>C(O)C>[CH2:1]([O:3][C:4]([N:6]1[CH2:7][CH2:8][N:9]([CH2:31][CH2:30][CH2:29][CH2:28][CH2:27][CH2:26][CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH3:17])[CH2:10][CH2:11]1)=[O:5])[CH3:2]

参加物

実験手順

25.0 Grams of 1-ethoxycarbonylpiperazine, 43.0 grams of pentadecyl methylsulfonate, 250 ml. of ethanol, and 9.53 grams of sodium carbonate are combined and heated to gentle reflux. After refluxing for 6 hours, the mixture is filtered, and the solvents removed under reduced pressure. The residue is dissolved in a mixture of water and ethyl ether. The organic layer is separated, washed once with water, and dried over anhydrous magnesium sulfate and anhydrous sodium sulfate. The solvent is removed under reduced pressure to give 1-ethoxycarbonyl-4-pentadecylpiperazine.