Citraconic Anhydrides → N-(5-bromopyridin-2-yl)-methylmaleimide

HRID 12146

反応式

HRID 12146 の反応式
[C:1]1(=[O:8])O[C:5](=[O:6])[CH:4]=[C:2]1[CH3:3].[NH2:9][C:10]1[CH:15]=[CH:14][C:13]([Br:16])=[CH:12][N:11]=1>C1(C)C=CC=CC=1>[Br:16][C:13]1[CH:14]=[CH:15][C:10]([N:9]2[C:5](=[O:6])[CH:4]=[C:2]([CH3:3])[C:1]2=[O:8])=[N:11][CH:12]=1

参加物

4

反応物 2

HCID 12012Citraconic AnhydridesHCID 706222-Amino-5-bromopyridine

生成物 1

HCID 22596423N-(5-bromopyridin-2-yl)-methylmaleimide収率 71%

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

A mixture of citraconic anhydride (1.00 mL, 11.1 mmol) and 2-amino-5-bromopyridine (1.93 g, 11.2 mmol) in toluene (60 mL) was heated to reflux overnight. The solution was cooled down, filtered. The filtrate was concentrated in vacuo to give a solid (2.10 g, yield: 71%). MS 267 and 269 (M+H).

後処理

  1. temperaturewas heated
  2. temperatureto reflux overnight
  3. temperatureThe solution was cooled down
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated in vacuo

出典と根拠

ORDレコード
ord-07517b26e624478c890fb3c51e114cc6
出典データセット
uspto-grants-2010_06
特許番号
US07727982B2

関連ノート

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