ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Agomelatine → N-(2-(7-hydroxy-1-naphthyl)ethyl)acetamide

HRID 1242678
ノート
印刷プレビュー

反応式

HRID 1242678 の反応式
C[O:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[CH:8][CH:9]=[C:10]2[CH2:13][CH2:14][NH:15][C:16](=[O:18])[CH3:17])=[CH:5][CH:4]=1>ClCCl>[OH:2][C:3]1[CH:12]=[C:11]2[C:6]([CH:7]=[CH:8][CH:9]=[C:10]2[CH2:13][CH2:14][NH:15][C:16](=[O:18])[CH3:17])=[CH:5][CH:4]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 82148Agomelatine

生成物 1

HCID 11775984N-(2-(7-hydroxy-1-naphthyl)ethyl)acetamide

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

Under an inert atmosphere, 27.5 mmol of boron tribromide/dimethyl sulphide complex are dissolved in 100 ml of dichloromethane and stirred for 15 min at ambient temperature. A solution of 13.7 mmol of N-[2-(7-methoxy-1-naphthyl)ethyl]acetamide in 50 ml of dichloromethane is added and the reaction mixture is heated at reflux for 30 hours. After cooling, the reaction mixture is hydrolysed with caution and the dichloromethane is evaporated off. The mixture is then extracted with ethyl acetate, the combined organic phases are washed with a 1M aqueous solution of potassium bicarbonate and then with 1M sodium hydroxide solution. The organic phase is dried over magnesium sulphate and concentrated to yield the title compound.

後処理

  • temperaturethe reaction mixture is heated
  • temperatureat reflux for 30 hours
  • temperatureAfter cooling
  • customthe dichloromethane is evaporated off
  • extractionThe mixture is then extracted with ethyl acetate
  • washthe combined organic phases are washed with a 1M aqueous solution of potassium bicarbonate
  • dry with materialThe organic phase is dried over magnesium sulphate
  • concentrationconcentrated
  • 出典と根拠

    ORDレコード
    ord-ca39becd5873457bba4a438f10e4364b
    出典データセット
    uspto-grants-2006_10
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07115752B2

    反応ノート

    読み込み中…

    このページの内容参加物実験手順後処理出典と根拠反応ノート