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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3-methyl-N-(1-methylethyl)-2-nitrobenzeneacetamide → 2-amino-3-methyl-N-(1-methylethyl)benzeneacetamide

HRID 905518
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인쇄 미리보기

반응식

HRID 905518 반응식
[CH3:1][C:2]1[C:3]([N+:15]([O-])=O)=[C:4]([CH2:8][C:9]([NH:11][CH:12]([CH3:14])[CH3:13])=[O:10])[CH:5]=[CH:6][CH:7]=1>[Pd].C(O)C>[NH2:15][C:3]1[C:2]([CH3:1])=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:8][C:9]([NH:11][CH:12]([CH3:14])[CH3:13])=[O:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 673911893-methyl-N-(1-methylethyl)-2-nitrobenzeneacetamide2회

생성물 1

HCID 673906992-amino-3-methyl-N-(1-methylethyl)benzeneacetamide

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

To 3-methyl-N-(1-methylethyl)-2-nitrobenzeneacetamide (i.e. the title product of Step A) (0.40 g, 1.7 mmol) and 10% palladium on carbon (0.13 g) was added 20 mL of ethanol. The reaction mixture was placed under a balloon of nitrogen overnight. Then the reaction mixture was filtered through Celite® diatomaceous filter aid. The solvent was removed with a rotary evaporator to afford the title compound as a tan solid (0.29 g).

후처리

  1. customwas placed under a balloon of nitrogen overnight
  2. filtrationThen the reaction mixture was filtered through Celite® diatomaceous filter aid
  3. customThe solvent was removed with a rotary evaporator

출처 및 근거

ORD 기록
ord-724fa7862a134c53b681cc5d9fd722e1
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08012499B2

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