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Methylamine → 4-Methylamino-3-nitroquinoline

HRID 580523
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인쇄 미리보기

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HRID 580523 반응식
Cl[C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][C:3]=1[N+:12]([O-:14])=[O:13].[CH3:15][NH2:16]>C(O)C>[CH3:15][NH:16][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[CH:4][C:3]=1[N+:12]([O-:14])=[O:13]
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참가 물질

4

반응물 2

HCID 6329MethylamineHCID 112758084-Chloro-3-nitroquinoline

생성물 1

HCID 139583214-Methylamino-3-nitroquinoline수율 93%

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

To a suspension of 2.0 g of 4-chloro-3-nitroquinoline in 20 ml of dry ethanol is added 15 ml of 30% methylamine in ethanol. The mixture is stirred at room temperature for 30 minutes and concentrated in vacuo. The residue is triturated with excess water. The resulting crystals are collected by filtration and washed repeatedly with water. The crystals are dried over phosphorus pentoxide in vacuo to afford 1.82 g (93%) of 4-methylamino-3-nitroquinoline.

후처리

  1. concentrationconcentrated in vacuo
  2. customThe residue is triturated with excess water
  3. filtrationThe resulting crystals are collected by filtration
  4. washwashed repeatedly with water
  5. dry with materialThe crystals are dried over phosphorus pentoxide in vacuo

출처 및 근거

ORD 기록
ord-a0273dc5255247159c8d25faa317f8ae
출처 데이터셋
uspto-grants-1988_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04753951

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