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5-bromo-2-methyl-3H-imidazo[4,5-b]pyridine → HCID 178432171、化合物

HRID 1699809
ノート
印刷プレビュー

反応式

HRID 1699809 の反応式
Br[C:2]1[N:7]=[C:6]2[N:8]=[C:9]([CH3:11])[NH:10][C:5]2=[CH:4][CH:3]=1.[Cu][C:13]#[N:14]>CN(C)C=O>[CH3:11][C:9]1[N:8]=[C:6]2[NH:7][C:2]([C:13]#[N:14])=[CH:3][CH:4]=[C:5]2[N:10]=1
参加物反応条件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 223879615-bromo-2-methyl-3H-imidazo[4,5-b]pyridineHCID 178418546HCID 178418546、化合物

生成物 1

HCID 178432171HCID 178432171、化合物収率 64.7%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
150 °C

実験手順

To a solution of 5-bromo-2-methyl-1H-imidazo[4,5-b]pyridine (1.92 g) in N,N-dimethylformamide (48 ml) was added Copper (I) cyanide (2.04 g), and the mixture was stirred for 9 hr at 150° C. After evaporation of the solvent under reduced pressure, water (45 ml) and ethylenediamine (2.7 g) were added to the residue, and the mixture was heated at 70° C. for 15 min. The solution was concentrated under reduced pressure and the residue was purified by a short silica gel column to give the objective compound (927 mg) as a brown powder. Purification by silica gel column chromatography (dichloromethane/methanol=10/1) gave a purer compound.

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. customAfter evaporation of the solvent under reduced pressure, water (45 ml) and ethylenediamine (2.7 g)
  2. additionwere added to the residue
  3. temperaturethe mixture was heated at 70° C. for 15 min
  4. concentrationThe solution was concentrated under reduced pressure
  5. customthe residue was purified by a short silica gel column

出典と根拠

ORDレコード
ord-bf714c75f6774bf59648cff94a937046
出典データセット
uspto-grants-2002_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06348474B1

反応ノート

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