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Methyl iodide → 6-Bromo-1-methyl-1h-indazol-4-amine

HRID 520594
ノート
印刷プレビュー

反応式

HRID 520594 の反応式
[Br:1][C:2]1[CH:3]=[C:4]([NH2:11])[C:5]2[CH:6]=[N:7][NH:8][C:9]=2[CH:10]=1.[H-].[Na+].[CH3:14]I>C1COCC1>[Br:1][C:2]1[CH:3]=[C:4]([NH2:11])[C:5]2[CH:6]=[N:7][N:8]([CH3:14])[C:9]=2[CH: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

5

反応物 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 247280636-Bromo-1H-indazol-4-amine

生成物 1

HCID 582557716-Bromo-1-methyl-1h-indazol-4-amine

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

6-Bromo-1H-indazol-4-amine (available from Sinova, 300 mg, 1.42 mmol) was dissolved in THF (7.5 ml) and the mixture cooled to 0° C. Sodium hydride (60% in mineral oil) (62 mg) was then slowly added. The mixture was stirred for 15 min, then methyl iodide (221 mg) was added and stirring continued at 0° C. for 3 h. The reaction mixture was quenched by careful addition of methanol (2 ml), then water (10 ml), then extracted into ethyl acetate and the organic layer was concentrated in vacuo. The residue was purified by column chromatography on silica eluting with a gradient of 0-50% ethyl acetate in cyclohexane. Fractions containing desired product were combined and concentrated in vacuo to afford the title compound, 48 mg.

後処理

  1. stirringstirring
  2. waitcontinued at 0° C. for 3 h
  3. customThe reaction mixture was quenched by careful addition of methanol (2 ml)
  4. extractionwater (10 ml), then extracted into ethyl acetate
  5. concentrationthe organic layer was concentrated in vacuo
  6. customThe residue was purified by column chromatography on silica eluting with a gradient of 0-50% ethyl acetate in cyclohexane
  7. additionFractions containing desired product
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-6a380060594c4b668618abdd9ef2cc78
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09326987B2

反応ノート

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