反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[CH:8]=[CH:9][C:10](=O)[NH:11][N:12]=1.O=P(Cl)(Cl)[Cl:16]>>[Cl:16][C:10]1[N:11]=[N:12][C:7]([C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][N:1]=2)=[CH:8][CH:9]=1参加物
3
実験手順
To a solid 6-pyridin-2-yl-2H-pyridazin-3-one (0.500 g, 2.900 mmol) was added 20 mL of POCl3 and the mixture was stirred at reflux for 4 hours. Excess POCl3 was removed in vacuo. The residue was poured on ice and neutralized using NaHCO3. The product was extracted with ether and ethyl acetate. The combined organic extracts were dried over MaSO4 and evaporated. The residue was purified by column chromatography to afford of 3-chloro-6-pyridin-2-ylpyridazine in 45% yield (0.250 g).
後処理
- temperatureat reflux for 4 hours
- customExcess POCl3 was removed in vacuo
- additionThe residue was poured on ice
- extractionThe product was extracted with ether and ethyl acetate
- customThe combined organic extracts were dried over MaSO4
- customevaporated
- customThe residue was purified by column chromatography
出典と根拠
- ORDレコード
- ord-8927cc31296542548e6cd2f7ab81a476
- 出典データセット
- uspto-grants-2010_08
- 特許番号
- US07767677B2
関連ノート
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