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

Phosphorus oxychloride → 7-Bromo-2-chloro-1,5-naphthyridine

HRID 509654
ノート
印刷プレビュー

反応式

HRID 509654 の反応式
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8](=O)[NH:9]2)=[N:4][CH:3]=1.O=P(Cl)(Cl)[Cl:15]>>[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH:6]=[CH:7][C:8]([Cl:15])=[N:9]2)=[N:4][CH:3]=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 2

HCID 24813Phosphorus oxychlorideHCID 57815430HCID 57815430、化合物

生成物 1

HCID 583105447-Bromo-2-chloro-1,5-naphthyridine収率 62.9%

実験手順

7-bromo-1,5-naphthyridin-2(1H)-one (C-4) (3.1 g, 13.78 mmol, 1.0 eq) was dissolved in POCl3 (20 mL) and the resulting mixture was stirred at reflux for 1 h. The reaction was complete based on TLC analysis. The mixture was concentrated in vacuo to remove POCl3. The residue was poured into ice water (30 mL) and neutralized with saturated aqueous Na2CO3 solution to adjust the pH value to 7-8 while keeping the temperature below 10° C. The resulting mixture was extracted with ethyl acetate (3×30 mL), the combined organic layer was washed with brine, dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo to afford the desired product 7-bromo-2-chloro-1,5-naphthyridine (F-31) (2.11 g, 62.9% yield). ESI-MS m/z: 242.9 [M+H]+.

後処理

  1. temperatureat reflux for 1 h
  2. concentration
The mixture was concentrated in vacuo
  • customto remove POCl3
  • additionThe residue was poured into ice water (30 mL)
  • customthe temperature below 10° C
  • extractionThe resulting mixture was extracted with ethyl acetate (3×30 mL)
  • washthe combined organic layer was washed with brine
  • dry with materialdried over Na2SO4
  • filtrationfiltered
  • concentrationThe filtrate was concentrated in vacuo
  • 出典と根拠

    ORDレコード
    ord-27a28933b9164875b84cbc516f4380af
    出典データセット
    uspto-grants-2015_08
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US09096590B2

    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