Acetic Acid → 3-iodo-1H-quinolin-2-one

HRID 381763ノート

反応式

HRID 381763 の反応式
Cl[C:2]1[C:11]([I:12])=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.C(O)(=[O:15])C>O>[I:12][C:11]1[C:2](=[O:15])[NH:3][C:4]2[C:9]([CH:10]=1)=[CH:8][CH:7]=[CH:6][CH:5]=2

参加物

4

反応物 2

HCID 176Acetic AcidHCID 146166232-Chloro-3-iodoquinoline

生成物 1

HCID 114145753-iodo-1H-quinolin-2-one

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
100 °C

実験手順

The 2-chloro-3-iodoquinoline (1-2, 30.0 g) was weighed into a 250 mL flask and suspended in of 50% aqueous acetic acid (125 mL). The mixture was heated to 100° C. and allowed to reflux for 16 h to completion by TLC analysis of the crude reaction mixture. The mixture was allowed to cool to ambient temperature followed by dilution with 200 mL of water. The resulting a suspension of the desired product was isolated by vacuum filtration follows by washing with water (50 mL). The water and traces of acetic acid were removed under vacuum for 5 h to afford the desired quinolinone as a tan powder (5-5); 1H NMR (500 MHz, CDCl3) δ12.13 (br s, 1H), 8.71 (s, 1H), 7.65 (d, 1H, J=7.5 Hz), 7.54 (m, 1H), 7.31 (d, 1H, J=8.0 Hz), 7.20 (m, 1H).

後処理

  1. temperatureto reflux for 16 h to completion by TLC analysis of the crude
  2. customreaction mixture
  3. temperatureto cool to ambient temperature

出典と根拠

ORDレコード
ord-d421f2a2e11743f5ac05bd6aaf456b50
出典データセット
uspto-grants-2001_10
特許番号
US06306874B1

反応ノート

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