Sodium Carbonate → 4-(1,2,3-thiadiazol-4-yl)pyridine
反応式
[C:1](=[N:9][NH:10]C(N)=O)([C:3]1[CH:8]=[CH:7][N:6]=[CH:5][CH:4]=1)[CH3:2].[S:14](Cl)(Cl)=O.C(=O)([O-])[O-].[Na+].[Na+]>C(Cl)(Cl)Cl>[S:14]1[CH:2]=[C:1]([C:3]2[CH:8]=[CH:7][N:6]=[CH:5][CH:4]=2)[N:9]=[N:10]1参加物
5
実験手順
16.8 g of 4-acetylpyridine semicarbazone was added to 47 ml of thionyl chloride under ice-cooling, and, after allowing to warm to room temperature, the mixture was stirred for 1 hour. 200 ml of chloroform was added to the reaction mixture, and the resulting mixture was added dropwise to an aqueous solution of sodium carbonate cooled with ice. The chloroform layer was separated, washed with water, dried and concentrated to obtain 3.4 g of 4-(1,2,3-thiadiazol-4-yl)pyridine. Melting point: 121°-123° C.
後処理
- temperaturecooling
- temperaturecooled with ice
- customThe chloroform layer was separated
- washwashed with water
- customdried
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-19d4b9ad136843178a319c19c55eddd8
- 出典データセット
- uspto-grants-1989_05
- 特許番号
- US04833242
反応ノート
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