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5-ethyl-1-(2-methoxyethyl)-4-nitro-1H-pyrazole-3-carboxamide → 4-amino-5-ethyl-1-(2-methoxyethyl)-1H-Pyrazole-3-carboxamide

HRID 47884
ノート
印刷プレビュー

反応式

HRID 47884 の反応式
[CH2:1]([C:3]1[N:7]([CH2:8][CH2:9][O:10][CH3:11])[N:6]=[C:5]([C:12]([NH2:14])=[O:13])[C:4]=1[N+:15]([O-])=O)[CH3:2]>CO.[Pd]>[NH2:15][C:4]1[C:5]([C:12]([NH2:14])=[O:13])=[N:6][N:7]([CH2:8][CH2:9][O:10][CH3:11])[C:3]=1[CH2:1][CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 112187175-ethyl-1-(2-methoxyethyl)-4-nitro-1H-pyrazole-3-carboxamide

生成物 1

HCID 112643124-amino-5-ethyl-1-(2-methoxyethyl)-1H-Pyrazole-3-carboxamide

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

A mixture of 5-ethyl-1-(2-methoxyethyl)-4-nitro-1H-pyrazole-3-carboxamide (20 g, 82.6 mMol) and 5%Pd/C (1 g) in methanol (200 mL) was pressurised at 50 psi/25° C. in a sealed vessel and stirred for 15 hours. At the end of the reaction the mixture was filtered through arbocel and the filter cake was washed with methanol. The methanolic solution was distilled at atmospheric pressure and replaced with ethyl acetate to a final volume of 100 mL. The cooled mixture was granulated at ambient temperature for 2 h filtered and washed with ethyl acetate (20 mL) to afford 4-amino-5-ethyl-1-(2-methoxyethyl)-1H-pyrazole-3-carboxamide as a white crystalline solid, 15 g, 88%. m.p.=131° C. Found: C, 50.75; H, 7.62; N, 26.38. C9H16N4O2 requires C, 50.94; H, 7.55; N, 26.42%.

後処理

  1. customwas pressurised at 50 psi/25° C. in a sealed vessel
  2. customAt the end of the reaction the mixture
  3. filtrationwas filtered through arbocel
  4. washthe filter cake was washed with methanol
  5. distillationThe methanolic solution was distilled at atmospheric pressure
  6. waitThe cooled mixture was granulated at ambient temperature for 2 h
  7. filtrationfiltered
  8. washwashed with ethyl acetate (20 mL)

出典と根拠

ORDレコード
ord-e67bc94a9a574addb96b61d708c3dd29
出典データセット
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06699991B2

反応ノート

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