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Iodoethane → 5-Ethoxy-1H-indazole

HRID 626328
ノート
印刷プレビュー

反応式

HRID 626328 の反応式
[OH:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][N:6]=[CH:5]2.[CH2:11](I)[CH3:12].C(=O)([O-])[O-].[K+].[K+]>CN(C=O)C>[CH2:11]([O:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][N:6]=[CH:5]2)[CH3:12]
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 3

HCID 6340IodoethaneHCID 11430Potassium CarbonateHCID 1014381H-Indazol-5-ol

生成物 1

HCID 220559665-Ethoxy-1H-indazole

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a solution of 5-hydroxyindazole (2.68 g) in DMF (50 mL) were added ethyl iodide (3.28 g) and potassium carbonate (4.16 g), and the mixture was stirred at room temperature for 1 day. Then, the mixture was partitioned between ethyl acetate and water, the organic layer was washed with brine and dried over Na2SO4, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate as the eluting solvent) to give Compound Q9 (1.95 g).

後処理

  1. customThen, the mixture was partitioned between ethyl acetate and water
  2. washthe organic layer was washed with brine
  3. dry with materialdried over Na2SO4
  4. customthe solvent was evaporated under reduced pressure
  5. customThe residue was purified by silica gel column chromatography (ethyl acetate as the eluting solvent)
  6. customto give Compound Q9 (1.95 g)

出典と根拠

ORDレコード
ord-242a489d50694377bb0a58bcad4f7f27
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09309221B2

反応ノート

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