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Butyl iodide → 5-Amino-2-butylpyrazol-3-carboxylic acid ethyl ester

HRID 240804
ノート
印刷プレビュー

反応式

HRID 240804 の反応式
[H-].[Na+].[CH2:3]([O:5][C:6]([C:8]1[CH:12]=[C:11]([NH2:13])[NH:10][N:9]=1)=[O:7])[CH3:4].[CH2:14](I)[CH2:15][CH2:16][CH3:17]>C(#N)C>[CH2:3]([O:5][C:6]([C:8]1[N:9]([CH2:14][CH2:15][CH2:16][CH3:17])[N:10]=[C:11]([NH2:13])[CH:12]=1)=[O:7])[CH3:4]
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 10962Butyl iodideHCID 24758Sodium hydrideHCID 178469278HCID 178469278、化合物

生成物 1

HCID 196199605-Amino-2-butylpyrazol-3-carboxylic acid ethyl ester収率 38%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

Sodium hydride (920 mg, 21 mmol) was added to a solution of 5-aminopyrazol-3-carboxylic acid ethyl ester (3.10 g, 20 mmol) in acetonitrile (100 mL) under a nitrogen atmosphere, and the obtained mixture was then stirred at room temperature for 30 minutes. The reaction solution was cooled on ice, and butyl iodide (2.3 mL, 20 mmol) was then added thereto. The obtained mixture was stirred at room temperature for 1 hour, and then at 60° C. for 1 hour. The reaction solution was left at room temperature overnight. Thereafter, the solvent was distilled away, and water was then added to the residue, followed by extraction with ethyl acetate. The organic layer was washed with water and a saturated saline, and it was dried over sodium sulfate and was then concentrated. The residue was purified by silica gel column chromatography (hexane/ethyl acetate), so as to obtain the title compound (1.60 g, yield: 38%) in the form of a pale yellow oily substance.

後処理

  1. additionwas then added
  2. stirringThe obtained mixture was stirred at room temperature for 1 hour
  3. waitat 60° C. for 1 hour
  4. waitThe reaction solution was left at room temperature overnight
  5. distillationThereafter, the solvent was distilled away
  6. additionwater was then added to the residue
  7. extractionfollowed by extraction with ethyl acetate
  8. washThe organic layer was washed with water
  9. dry with materiala saturated saline, and it was dried over sodium sulfate
  10. concentrationwas then concentrated
  11. customThe residue was purified by silica gel column chromatography (hexane/ethyl acetate)

出典と根拠

ORDレコード
ord-6214083c5f57462b8e51a6122546e5fb
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08648103B2

反応ノート

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