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1-(4-(3-Ethoxy-4-nitrophenyl)piperazin-1-yl)ethanone → 1-(4-(4-Amino-3-ethoxyphenyl)piperazin-1-yl)ethanone

HRID 1496946
ノート
印刷プレビュー

反応式

HRID 1496946 の反応式
[CH2:1]([O:3][C:4]1[CH:5]=[C:6]([N:13]2[CH2:18][CH2:17][N:16]([C:19](=[O:21])[CH3:20])[CH2:15][CH2:14]2)[CH:7]=[CH:8][C:9]=1[N+:10]([O-])=O)[CH3:2]>C(O)C.[Pd]>[NH2:10][C:9]1[CH:8]=[CH:7][C:6]([N:13]2[CH2:18][CH2:17][N:16]([C:19](=[O:21])[CH3:20])[CH2:15][CH2:14]2)=[CH:5][C:4]=1[O:3][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 1181057541-(4-(3-Ethoxy-4-nitrophenyl)piperazin-1-yl)ethanone

生成物 1

HCID 636720981-(4-(4-Amino-3-ethoxyphenyl)piperazin-1-yl)ethanone

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 702Ethanol溶媒

実験手順

The compound prepared in Step 2 was dissolved in ethanol, added with 10% Pd/C and stirred under hydrogen atmosphere for 2 hours. Upon completion of the reaction, the Pd/C in the reaction mixture was removed using celite and the solvent was removed under reduced pressure. The thus obtained compound was used in the subsequent reaction without further purification.

後処理

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
  1. customUpon completion of the reaction
  2. customthe Pd/C in the reaction mixture was removed
  3. customthe solvent was removed under reduced pressure
  4. customThe thus obtained compound was used in the subsequent reaction without further purification

出典と根拠

ORDレコード
ord-256635da0a55413c891fd2a1c178274a
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09199944B2

反応ノート

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