1,1'-Biphenyl, mixt. with 1,1'-oxybis(benzene) → Ethyl 8-chloro-4-oxo-5-(trifluoromethyl)-1,4-dihydroquinoline-3-carboxylate

HRID 400979ノート

反応式

HRID 400979 の反応式
C1C=CC(C2C=CC=CC=2)=CC=1.C1C=CC(OC2C=CC=CC=2)=CC=1.[Cl:26][C:27]1[CH:32]=[CH:31][C:30]([C:33]([F:36])([F:35])[F:34])=[CH:29][C:28]=1[NH:37][CH:38]=[C:39]([C:45](OCC)=[O:46])[C:40]([O:42][CH2:43][CH3:44])=[O:41]>>[Cl:26][C:27]1[CH:32]=[CH:31][C:30]([C:33]([F:34])([F:35])[F:36])=[C:29]2[C:28]=1[NH:37][CH:38]=[C:39]([C:40]([O:42][CH2:43][CH3:44])=[O:41])[C:45]2=[O:46]

参加物

3

反応条件

温度
260 °C

実験手順

A 3-neck, 1 L flask was charged with Dowtherm® (200 mL, 8 mL/g), and was degassed at 200° C. for 1 h. The solvent was heated to 260° C. and charged in portions over 10 minutes (min) with diethyl 2-((2-chloro-5-(trifluoromethyl)phenylamino) methylene)malonate (4) (25 g, 0.07 mol). The resulting mixture was stirred at 260° C. for 6.5 h and the resulting ethanol byproduct removed by distillation. The mixture was allowed to slowly cool to 80° C. Hexane (150 mL) was slowly added over 30 min, followed by an additional 200 mL of hexane added in one portion. The slurry was stirred until it had reached room temperature. The solid was filtered, washed with hexane (3×150 mL), and then dried under vacuum to provide ethyl 8-chloro-4-oxo-5-(trifluoromethyl)-1,4-dihydroquinoline-3-carboxylate (5A) as a tan solid. 1H NMR (400 MHz, DMSO-d6) δ 11.91 (s, 1H), 8.39 (s, 1H), 8.06 (d, J=8.3 Hz, 1H), 7.81 (d, J=8.4 Hz, 1H), 4.24 (q, J=7.1 Hz, 2H), 1.29 (t, J=7.1 Hz, 3H).

後処理

  1. customwas degassed at 200° C. for 1 h
  2. customthe resulting ethanol byproduct removed by distillation
  3. temperatureto slowly cool to 80° C
  4. additionHexane (150 mL) was slowly added over 30 min
  5. additionadded in one portion
  6. stirringThe slurry was stirred until it
  7. customhad reached room temperature
  8. filtrationThe solid was filtered
  9. washwashed with hexane (3×150 mL)
  10. customdried under vacuum

出典と根拠

ORDレコード
ord-4c717a8db2d34e98bdb9a57a3d2c8cf4
出典データセット
uspto-grants-2014_06
特許番号
US08741922B2

反応ノート

読み込み中…