m-Chloroperbenzoic acid → HCID 178437532、化合物

HRID 466712

反応式

HRID 466712 の反応式
[CH2:1]([C:3]1[NH:4][C:5]2[C:6]([N:12]=1)=[N:7][CH:8]=[CH:9][C:10]=2[CH3:11])[CH3:2].ClC1C=CC=C(C(OO)=[O:21])C=1>C(Cl)(Cl)Cl>[CH2:1]([C:3]1[NH:4][C:5]2[C:6]([N:12]=1)=[N+:7]([O-:21])[CH:8]=[CH:9][C:10]=2[CH3:11])[CH3:2]

参加物

4

反応物 2

HCID 70297m-Chloroperbenzoic acidHCID 186930362-ethyl-7-methyl-3H-Imidazo[4,5-b]pyridine

生成物 1

HCID 178437532HCID 178437532、化合物収率 96.6%

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

A solution of 2-ethyl-7-methylimidazo[4,5-b]pyridine (28 g, 174 mmol) and m-chloroperbenzoic acid (80-90%, 44.6 g) in CHCl3 (300 mL) was heated at reflux for 0.5 hours. The mixture was concentrated and purified (SiO2, 100% CH2Cl2 gradient to 30% CH2Cl2 /MeOH) to give 29.8 g of 2-ethyl-7-methylimidazo[4,5-b]pyridine-4-oxide as a solid.

後処理

  1. temperatureat reflux for 0.5 hours
  2. concentrationThe mixture was concentrated
  3. custompurified (SiO2, 100% CH2Cl2 gradient to 30% CH2Cl2 /MeOH)

出典と根拠

ORDレコード
ord-cd37bc5a7a2c44379e6b18f4b6ffcc55
出典データセット
uspto-grants-1992_10
特許番号
US05157026

関連ノート

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