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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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methyl 1-methyl-5-nitro-1H-pyrazole-3-carboxylate → methyl 5-amino-1-methyl-1H-pyrazole-3-carboxylate

HRID 541428
ノート
印刷プレビュー

反応式

HRID 541428 の反応式
[CH3:1][N:2]1[C:6]([N+:7]([O-])=O)=[CH:5][C:4]([C:10]([O:12][CH3:13])=[O:11])=[N:3]1>CO.[Pd]>[NH2:7][C:6]1[N:2]([CH3:1])[N:3]=[C:4]([C:10]([O:12][CH3:13])=[O:11])[CH:5]=1
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 50896836methyl 1-methyl-5-nitro-1H-pyrazole-3-carboxylate

生成物 1

HCID 13324840methyl 5-amino-1-methyl-1H-pyrazole-3-carboxylate収率 90%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

To a solution of methyl 1-methyl-5-nitro-1H-pyrazole-3-carboxylate (351.2, 0.48 g, 2.60 mmol) in MeOH (15 ml) under nitrogen was added palladium on carbon (10%, 0.25 g). The flask was further degassed with nitrogen and filled with H2 through a balloon. The mixture was stirred at room temperature for 1.5 hours. After purging the system with nitrogen, the reaction mixture was filtered through a Celite cake and concentrated to give 363 mg (90%) of a white solid. m/z (ES+) 156 (M+H)+.

後処理

  1. customThe flask was further degassed with nitrogen
  2. additionfilled with H2 through a balloon
  3. customAfter purging the system with nitrogen
  4. filtrationthe reaction mixture was filtered through a Celite cake
  5. concentrationconcentrated

出典と根拠

ORDレコード
ord-a816c534cab34aa99d425cc78aa7ee08
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08871790B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート