Water → 2-(4-Chlorophenyl)-6H,7H-thieno[2,3-c]pyridin-7-one

HRID 2384877ノート

反応式

HRID 2384877 の反応式
FC(F)(F)S(O)(=O)=O.O=[CH:10][CH2:11][NH:12][C:13]([C:15]1[S:16][C:17]([C:20]2[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][CH:21]=2)=[CH:18][CH:19]=1)=[O:14].O>>[Cl:26][C:23]1[CH:24]=[CH:25][C:20]([C:17]2[S:16][C:15]3[C:13](=[O:14])[NH:12][CH:11]=[CH:10][C:19]=3[CH:18]=2)=[CH:21][CH:22]=1

参加物

4

反応物 3

HCID 962WaterHCID 62406Trifluoromethanesulfonic acidHCID 866292045-(4-Chlorophenyl)-thiophene-2-carboxylic acid (2-oxoethyl)amide

生成物 1

HCID 576495192-(4-Chlorophenyl)-6H,7H-thieno[2,3-c]pyridin-7-one収率 100%

反応条件

温度
95 °C

実験手順

Add trifluoromethane sulfonic acid (3 mL, 0.03 mol) and 5-(4-chlorophenyl)-thiophene-2-carboxylic acid (2-oxoethyl) amide (1 g, 0.004 mol) to a 25 mL three-necked round bottom flask equipped with a stir bar, Dean-Stark trap, nitrogen inlet/outlet, and thermocouple. Heat the reaction mixture to 95° C. for 2 h, then cool to 40° C., and pour onto cold water (20 mL, 1.11 mol). Stir the mixture for 10 min. Filter the resulting slurry and rinse the solids with water (100 mL). Dry to afford crude 2-(4-chlorophenyl)-6H-thieno[2,3-c]pyridine-7-one (0.95 g, 0.004 mol) as a brown solid. LC-MS/ES m/z (35Cl) 262 [M+1]+.

後処理

  1. customequipped with a stir bar
  2. temperaturecool to 40° C.
  3. filtrationFilter the resulting slurry
  4. washrinse the solids with water (100 mL)
  5. customDry

出典と根拠

ORDレコード
ord-b16b44aeeb7f4af8b1841efd9275d9ea
出典データセット
uspto-grants-2012_09
特許番号
US08263772B2

反応ノート

読み込み中…