Methanol → HCID 178484914、化合物

反応式

[ClH:1].C1(=O)[N:6]([CH2:7][C:8]2[CH:13]=[CH:12][C:11]([CH2:14][CH2:15][C:16]3[CH:25]=[CH:24][C:19]([C:20](=[NH:23])OC)=[CH:18][CH:17]=3)=[CH:10][CH:9]=2)[C:5](=[O:26])[C:4]2=[CH:27][CH:28]=[CH:29][CH:30]=[C:3]12.[CH3:32][OH:33].[CH3:34][NH2:35].CCOCC>C(Cl)(Cl)Cl>[ClH:1].[CH3:34][NH:35][C:20](=[NH:23])[C:19]1[CH:18]=[CH:17][C:16]([CH2:15][CH2:14][C:11]2[CH:12]=[CH:13][C:8]([CH2:7][N:6]3[C:32](=[O:33])[C:27]4=[CH:28][CH:29]=[CH:30][CH:3]=[C:4]4[C:5]3=[O:26])=[CH:9][CH:10]=2)=[CH:25][CH:24]=1

参加物

実験手順

To a solution of 1.5 g of methyl 4-[2-(4-phthalimidomethylphenyl)ethyl]benzimidate hydrochloride in 150 ml of chloroform, was added 0.3 ml of a methanol solution containing 40% of methylamine. The mixture was stirred at room temperature for 15 hours. The reaction mixture was stripped of the solvent under reduced pressure. Ether was added to the residue and the precipitated crystals were collected by filtration to yield 1.3 g of N-methyl-4-[2-(4-phthalimidomethylphenyl)ethyl]benzamidine hydrochloride; m.p. 270° C. or above.