反応式
CN(C)C=O.[C:6]([C:8]1[CH:13]=[N:12][CH:11]=[CH:10][N:9]=1)#[N:7].S(Cl)([Cl:17])(=O)=O>C1C=CC=CC=1>[Cl:17][C:13]1[C:8]([C:6]#[N:7])=[N:9][CH:10]=[CH:11][N:12]=1参加物
実験手順
In 90 ml of benzene and 9.2 ml of dimethylformamide there was stirred at room temperature cyanopyrazine (12.7 g; 0.12 M) prepared in Step A above, after which there was added over 10 minutes sulfonyl chloride (64.79 g; 0.48 M). The reaction mixture was stirred for 30 minutes in an ice bath, then allowed to warm up to room temperature gradually, after which it was stirred for 5 hours. The benzene layer was decanted, and the reddish oil residue was extracted three times with ether, after which the combined benzene and ether layers were quenched with ice water and cooled in an ice bath. The combined layers were then neutralized with solid sodium bicarbonate, then separated, and the aqueous layer was extracted with ether. The combined organic layers were washed once with a small amount of water, dried with sodium sulfate, filtered, and the solvent evaporated to give the title compound (11 g).
後処理
- customprepared in Step A above
- stirringafter which it was stirred for 5 hours
- customThe benzene layer was decanted
- extractionthe reddish oil residue was extracted three times with ether
- customafter which the combined benzene and ether layers were quenched with ice water
- temperaturecooled in an ice bath
- customseparated
- extractionthe aqueous layer was extracted with ether
- washThe combined organic layers were washed once with a small amount of water
- dry with materialdried with sodium sulfate
- filtrationfiltered
- customthe solvent evaporated
出典と根拠
- ORDレコード
- ord-733bffbef1bf4c24911690a97d3791a7
- 出典データセット
- uspto-grants-1984_04
- 特許番号
- US04442095
関連ノート
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