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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
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인쇄 미리보기

반응식

HRID 1496946 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 1181057541-(4-(3-Ethoxy-4-nitrophenyl)piperazin-1-yl)ethanone

생성물 1

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

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

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.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  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

출처 및 근거

ORD 기록
ord-256635da0a55413c891fd2a1c178274a
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09199944B2

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