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

Bromine → 3-Bromo-2-ethyl-imidazo[1,2-a]pyridine

HRID 1357931
ノート
印刷プレビュー

反応式

HRID 1357931 の反応式
[CH2:1]([C:3]1[N:4]=[C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][N:6]2[CH:11]=1)[CH3:2].[Br:12]Br>C(O)C.O>[Br:12][C:11]1[N:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]2=[N:4][C:3]=1[CH2:1][CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 24408BromineHCID 218319912-Ethylimidazo[1,2-a]pyridine

生成物 1

HCID 219127413-Bromo-2-ethyl-imidazo[1,2-a]pyridine収率 66.8%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒2 回HCID 962Water溶媒

実験手順

To a solution of 2-ethyl-imidazo[1,2-a]pyridine (2.17 g, 14.9 mmol) in ethanol (25 mL) was added bromine (2.0 g, 12.5 mmol) in water (5 mL) dropwise at rt. After stirring at rt for 4h, ethanol was evaporated under reduced pressure. The residue was basified with aqueous sodium bicarbonate and extracted with methylene chloride (3×). The organic phase was washed with brine and dried over anhydrous magnesium sulfate. Concentration followed by flash chromatography eluting with 20 % ethyl acetate in hexanes, followed by 50% ethyl acetate in hexanes afforded the title compound (1.88 g) as a viscous oil.

後処理

  1. customwas evaporated under reduced pressure
  2. extractionextracted with methylene chloride (3×)
  3. washThe organic phase was washed with brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationConcentration
  6. washeluting with 20 % ethyl acetate in hexanes

出典と根拠

ORDレコード
ord-561312f5aed24479b2ebee4db8301ee2
出典データセット
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06593346B2

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