2-Amino-4-chlorobenzenethiol → 5-Chloro-2-(pyridin-4-yl)-1,3-benzothiazole
反応式
[NH2:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[CH:4][C:3]=1[SH:9].[N:10]1[CH:15]=[CH:14][C:13]([CH:16]=O)=[CH:12][CH:11]=1>>[Cl:8][C:6]1[CH:5]=[CH:4][C:3]2[S:9][C:16]([C:13]3[CH:14]=[CH:15][N:10]=[CH:11][CH:12]=3)=[N:1][C:2]=2[CH:7]=1参加物
3
実験手順
2-Amino-4-chlorothiophenol (6.5 g, 0.04 mol) and 4-pyridine carboxaldehyde (4.4. g, 0.04 mol) were reacted as exemplified in Example 7 step 1, to afford the title compound as a brown solid (1.8 g, 20%). δH (CDCl3), 7.44 (1H, m, ArH), 7.86 (1H, m, ArH), 7.92 (2H, m, ArH), 8.08 (1H, s, ArH), 8.78 (2H, m, ArH). m/z (ES+) 247 (M+1)+.
出典と根拠
- ORDレコード
- ord-a8c7b0fc6d884789ade468f73733b5f8
- 出典データセット
- uspto-grants-1998_12
- 特許番号
- US05849765
反応ノート
読み込み中…