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Dimethylamine → 4-Dimethylamino-2-nitro-N-quinolin-8-yl-benzenesulfonamide

HRID 513760
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HRID 513760 반응식
F[C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH:11][C:12]2[CH:13]=[CH:14][CH:15]=[C:16]3[C:21]=2[N:20]=[CH:19][CH:18]=[CH:17]3)(=[O:10])=[O:9])=[C:4]([N+:22]([O-:24])=[O:23])[CH:3]=1.[CH3:25][NH:26][CH3:27]>O>[CH3:25][N:26]([CH3:27])[C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH:11][C:12]2[CH:13]=[CH:14][CH:15]=[C:16]3[C:21]=2[N:20]=[CH:19][CH:18]=[CH:17]3)(=[O:10])=[O:9])=[C:4]([N+:22]([O-:24])=[O:23])[CH:3]=1
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참가 물질

4

반응물 2

HCID 674DimethylamineHCID 167599244-Fluoro-2-nitro-N-quinolin-8-yl-benzenesulfonamide

생성물 1

HCID 681833904-Dimethylamino-2-nitro-N-quinolin-8-yl-benzenesulfonamide수율 97%

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
90 °C

실험 절차

4-Fluoro-2-nitro-N-quinolin-8-yl-benzenesulfonamide 145 (0.13 g, 0.36 mmol) was dissolved in dimethyl amine (2M in THF; 1.77 ml, 3.59 mmol) and the mixture was heated at 90° C. in a sealed tube for 5 h. After cooling, water was added and the mixture was extracted with EtOAc. The organic phase was dried (Na2SO4) and concentrated in vacuo to give the title compound (0.13 g, 97%) which was used in the next step without further purification.

후처리

  1. temperatureAfter cooling
  2. extractionthe mixture was extracted with EtOAc
  3. dry with materialThe organic phase was dried (Na2SO4)
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-46812e160dd3498f8ebcb1bfe2d53345
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09102688B2

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