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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-Methylamino-3-nitroquinoline → 3-Amino-4-(methylamino)quinoline

HRID 580524
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인쇄 미리보기

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HRID 580524 반응식
[CH3:1][NH:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[N:6]=[CH:5][C:4]=1[N+:13]([O-])=O>C(O)C.[Pd]>[NH2:13][C:4]1[CH:5]=[N:6][C:7]2[C:12]([C:3]=1[NH:2][CH3:1])=[CH:11][CH:10]=[CH:9][CH:8]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 139583214-Methylamino-3-nitroquinoline

생성물 1

HCID 139583463-Amino-4-(methylamino)quinoline수율 41.4%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A suspension of 1.7 g of 4-methylamino-3-nitroquinoline in 75 ml of ethanol is hydrogenated in the presence of 300 mg of 10% palladium on carbon at atmospheric pressure. After hydrogen absorption is complete, the catalyst is removed by filtration and the filtrate is concentrated in vacuo. The residue is purified by column chromatography on silica gel. Elution with chloroform-methanol (2:1 v/v) affords 600 mg (41%) of 3-amino-4-methylaminoquinoline A15 as an oil.

후처리

  1. customAfter hydrogen absorption
  2. customthe catalyst is removed by filtration
  3. concentrationthe filtrate is concentrated in vacuo
  4. customThe residue is purified by column chromatography on silica gel
  5. washElution with chloroform-methanol (2:1 v/v)

출처 및 근거

ORD 기록
ord-025ef8fb61934d759fc6cef98b1fbb90
출처 데이터셋
uspto-grants-1988_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04753951

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