Oxalic Acid → N,N-Diethyl-N'-[2-(phenylsulfonyl)ethyl]-1,4-butanediamine oxalate hydrate

反応式

Cl[CH2:2][CH2:3][S:4]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)(=[O:6])=[O:5].[CH2:13]([N:15]([CH2:18][CH2:19][CH2:20][CH2:21][NH2:22])[CH2:16][CH3:17])[CH3:14].[C:23]([OH:28])(=[O:27])[C:24]([OH:26])=[O:25]>C(#N)C>[OH2:5].[C:23]([OH:28])(=[O:27])[C:24]([OH:26])=[O:25].[CH2:13]([N:15]([CH2:16][CH3:17])[CH2:18][CH2:19][CH2:20][CH2:21][NH:22][CH2:2][CH2:3][S:4]([C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)(=[O:6])=[O:5])[CH3:14]

参加物

実験手順

A mixture of 28.2 g (0.138 mole) of [(2-chloroethyl)sulfonyl]benzene and 20.0 g (0.139 mole) of 4-(N,N-diethylamino)-1-butanamine in 700 ml of acetonitrile was stirred at room temperature for 16 hr. The solvent was removed in vacuo, and the residue was partitioned between methylene chloride and dilute sodium hydroxide. The methylene chloride solution was dried over magnesium sulfate, and the solvent was removed in vacuo. The residue was dissolved in methanol, a solution of 25.0 g (0.278 mole) of oxalic acid was added and a precipitate was collected to give 47.69 g (68.9%) of title compound, a white crystalline solid, mp 158°-165° C. with decomposition.