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

Stannous chloride dihydrate → 6-Bromo-7-fluoro-3,4-dihydroquinoxalin-2(1H)-one

HRID 1857397
ノート
印刷プレビュー

反応式

HRID 1857397 の反応式
[Na+].[Br:2][C:3]1[C:4]([F:17])=[CH:5][C:6]([N+:14]([O-])=O)=[C:7]([NH:9][CH2:10][C:11]([O-])=[O:12])[CH:8]=1.O.O.[Sn](Cl)Cl>C(O)C>[Br:2][C:3]1[CH:8]=[C:7]2[C:6](=[CH:5][C:4]=1[F:17])[NH:14][C:11](=[O:12])[CH2:10][NH:9]2
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 61436Stannous chloride dihydrateHCID 15194586HCID 15194586、化合物

生成物 1

HCID 100604066-Bromo-7-fluoro-3,4-dihydroquinoxalin-2(1H)-one

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A solution of N-(5'-bromo-4'-fluoro-2'-nitrophenyl)glycine sodium salt (0.450 g, 1.54 mmol, as prepared above) and tin (II) chloride dihydrate (1.039 g, 4.605 mmol, Aldrich, used as received) in ethanol (7.0 mL) was refluxed for 30 min. It was then cooled to room temperature and solvent was removed under vacuum. The residue was diluted with water (15.0 mL) and basified with 10% Na2CO3 to pH~8. The resulting suspension was extracted with ethyl acetate (100 mL). The ethyl acetate was dried over anhydrous Na2SO4 and removed under vacuum to yield 0.241 g (64%).of the title compound as a yellow powder, m.p. 214-216° C.; 1H NMR (DMSO-d6): δ 3.684 (s, 2H), 6.062 (s, 1H), 6.631 (d, 1H, J=9.3 Hz), 6.825 (d, 1H, J=6.6 Hz), 10.303 (s, 1H).

後処理

  1. customsolvent was removed under vacuum
  2. additionThe residue was diluted with water (15.0 mL)
  3. extractionThe resulting suspension was extracted with ethyl acetate (100 mL)
  4. dry with materialThe ethyl acetate was dried over anhydrous Na2SO4
  5. customremoved under vacuum
  6. customto yield 0.241 g (64%)

出典と根拠

ORDレコード
ord-b5c83dead65749e0943377f8a0fb3107
出典データセット
uspto-grants-2000_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06147075

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