Water → HCID 19854544、化合物

HRID 1649718ノート

反応式

HRID 1649718 の反応式
[C:1]([NH:4][C:5]1[CH:18]=[CH:17][C:8]([C:9]([CH:11]([CH3:16])[CH2:12][C:13]([OH:15])=[O:14])=[O:10])=[CH:7][CH:6]=1)(=[O:3])[CH3:2].[H-].[Na+].Br[CH2:22][CH2:23][CH2:24][N:25]1[C:29](=[O:30])[C:28]2=[CH:31][CH:32]=[CH:33][CH:34]=[C:27]2[C:26]1=[O:35].O>CS(C)=O>[C:26]1(=[O:35])[N:25]([CH2:24][CH2:23][CH2:22][N:4]([C:5]2[CH:18]=[CH:17][C:8]([C:9]([CH:11]([CH3:16])[CH2:12][C:13]([OH:15])=[O:14])=[O:10])=[CH:7][CH:6]=2)[C:1](=[O:3])[CH3:2])[C:29](=[O:30])[C:28]2=[CH:31][CH:32]=[CH:33][CH:34]=[C:27]12

参加物

6

反応条件

温度
60 °C

実験手順

30.0 g (120 mmol) of 3-(4-acetamidobenzoyl)-butyric acid are added to a suspension of 7.6 g (253 mmol) of sodium hydride (80%) in 150 ml of dimethyl sulphoxide and the mixture is stirred for 30 minutes at 60° C. After the addition of 33.2 g (120 mmol) of N-(3-bromopropyl)-phthalimide, stirring is continued at 80° C. for 6 hours. After cooling, the reaction mixture is poured out on 200 ml of iced water and extracted with 3×100 ml of dichloromethane. The extracts are discarded. The aqueous phase is then adjusted to pH 6.5 with 2N hydrochloric acid and again extracted with 3×100 ml of dichloromethane. The combined organic phases are dried and concentrated by evaporation under vacuum. The oil obtained as residue crystallizes when triturated with 20 ml of ethanol.

後処理

  1. stirringstirring
  2. waitis continued at 80° C. for 6 hours
  3. temperatureAfter cooling
  4. extractionextracted with 3×100 ml of dichloromethane
  5. extractionagain extracted with 3×100 ml of dichloromethane
  6. customThe combined organic phases are dried
  7. concentrationconcentrated by evaporation under vacuum
  8. customThe oil obtained as residue
  9. customcrystallizes when
  10. customtriturated with 20 ml of ethanol

出典と根拠

ORDレコード
ord-29bc8c2eef6748ffbafbb550c6324269
出典データセット
uspto-grants-1990_05
特許番号
US04921856

反応ノート

読み込み中…