反応式
Cl.NC1NC=C(CO)N=1.C1(C([O-])=C([N+]([O-])=O)C=C([N+]([O-])=O)C=1)[N+]([O-])=O.Cl.Cl.NCCS.[NH2:32][C:33]1[NH:34][CH:35]=[C:36]([CH2:38][S:39][CH2:40][CH2:41][NH2:42])[N:37]=1.[N+:43]([CH:46]=[C:47](SC)[S:48][CH3:49])([O-:45])=[O:44]>>[N+:43]([CH:46]=[C:47]([S:48][CH3:49])[NH:42][CH2:41][CH2:40][S:39][CH2:38][C:36]1[N:37]=[C:33]([NH2:32])[NH:34][CH:35]=1)([O-:45])=[O:44]参加物
7
実験手順
Reaction of 2-amino-4-hydroxymethylimidazole hydrochloride (which is obtained by treating the picrate salt with hydrochloric acid) with cysteamine hydrochloride and reaction of the resulting 2-amino-4-[(2-aminoethyl)thiomethyl]imidazole with 1-nitro-2,2-bis-methylthioethylene according to the procedure of Example 8(i) gives 1-nitro-2-methylthio-2-[2-((2-amino-4-imidazolyl)methylthio)ethylamino]ethylene. Finally, reaction with methylamine by the procedure of Example 8(ii) produces the title compound.
後処理
- customis obtained
出典と根拠
- ORDレコード
- ord-36af4469352d4837ba1f2dc05aba61b9
- 出典データセット
- uspto-grants-1979_05
- 特許番号
- US04153704
関連ノート
読み込み中…