Water → N-Methyl-8-nitroquinolin-7-amine

HRID 1772000노트

반응식

HRID 1772000 반응식
[N+:1]([C:4]1[C:5]([NH2:14])=[CH:6][CH:7]=[C:8]2[C:13]=1[N:12]=[CH:11][CH:10]=[CH:9]2)([O-:3])=[O:2].[H-].[Na+].I[CH3:18].O>O1CCCC1>[CH3:18][NH:14][C:5]1[C:4]([N+:1]([O-:3])=[O:2])=[C:13]2[C:8]([CH:9]=[CH:10][CH:11]=[N:12]2)=[CH:7][CH:6]=1

참가 물질

6

반응물 4

HCID 962WaterHCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 129549938-Nitroquinolin-7-amine

생성물 1

HCID 29985233N-Methyl-8-nitroquinolin-7-amine수율 79%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 8-nitroquinolin-7-amine (1.89 g, 10 mmol) in tetrahydrofuran (THF) (10 mL) was added sodium hydride (60% wt in mineral oil, 800 mg, 20 mmol). The mixture was stirred at room temperature for 30 minutes, then iodomethane (1.42 g, 10 mmol) was added. The mixture was stirred at room temperature for 5 h. Then water (10 mL) was added. The mixture was extracted with EtOAc, and the organic layer was concentrated. The residue was purified by silica gel column chromatography (eluting with PE/EtOAc v/v 2:1) to give N-methyl-8-nitroquinolin-7-amine as a yellow solid (1.6 g, yield 79%). ESI MS: m/z 204 [M+H]+.

후처리

  1. stirringThe mixture was stirred at room temperature for 5 h
  2. extractionThe mixture was extracted with EtOAc
  3. concentrationthe organic layer was concentrated
  4. customThe residue was purified by silica gel column chromatography (
  5. washeluting with PE/EtOAc v/v 2:1)

출처 및 근거

ORD 기록
ord-a5574104e15c45fea88c47f82c713a9a
출처 데이터셋
uspto-grants-2016_02
특허 번호
US09249162B2

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