反応式
[CH3:1][I:2].[NH2:3][C:4]1[S:5][C:6]([CH3:9])=[N:7][N:8]=1>C(O)(C)C>[IH:2].[NH:3]=[C:4]1[N:8]([CH3:1])[N:7]=[C:6]([CH3:9])[S:5]1参加物
4
実験手順
64.1 g of methyl iodide are added to a solution of 17.6 g of 2-amino-5-methyl-1,3,4-thiadiazole in 350 ml isopropanol. The solution is refluxed for 15 hours. The reaction mixture is then evaporated to dryness, the crystalline evaporation residue is stirred with ethyl acetate and the solvent is filtered off with suction. The crystalline residue is washed, first with ethyl acetate and then with ether, and then dried. 2-Imino-3,5-dimethyl-4-(1,3,4) -thiadiazoline hydroiodide with a melting point of 208° (decomposition) is thus obtained.
後処理
- temperatureThe solution is refluxed for 15 hours
- customThe reaction mixture is then evaporated to dryness
- filtrationthe solvent is filtered off with suction
- washThe crystalline residue is washed, first with ethyl acetate
- dry with materialwith ether, and then dried
出典と根拠
- ORDレコード
- ord-bf3f6cd9eeb340b9976ab9527da93279
- 出典データセット
- uspto-grants-1982_08
- 特許番号
- US04342764
関連ノート
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