Amantadine → 3-Adamant-1-ylcarbamoyl-1,2,4-oxadiazole
反応式
[N:1]([C:4]([C:6]1[N:10]=[CH:9][O:8][N:7]=1)=[O:5])=[N+]=[N-].N[C:12]12[CH2:21][CH:16]3[CH2:17][CH:18]([CH2:20][CH:14]([CH2:15]3)[CH2:13]1)[CH2:19]2>C(Cl)(Cl)Cl>[C:12]12([NH:1][C:4]([C:6]3[N:10]=[CH:9][O:8][N:7]=3)=[O:5])[CH2:21][CH:16]3[CH2:17][CH:18]([CH2:20][CH:14]([CH2:15]3)[CH2:13]1)[CH2:19]2参加物
4
実験手順
3-Azidocarbonyl-1,2,4-oxadiazole (350 mg.) was added to a solution of 1-aminoadamantane (378 mg.) in chloroform (15 ml.) and the mixture was stirred for 24 hr. The chloroform solution was evaporated to dryness under reduced pressure and the residue was recrystallised from aqueous methanol to give title compound (167 mg.), m.p. 141°-142°, νmax. (EtOH) 230 nm (ε 3,910), λmax. (Nujol) 3392 (--NH--) 1692 and 1515 cm.-1 (CONH). Further examples provided in Table II were prepared by the following general methods: