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Dimethylformamide → 2-(4-Aminophenylsulfinyl)quinoline

HRID 2395343
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반응식

HRID 2395343 반응식
[N+](C1C=CC([C:10]2[C:11]([S:20](C3C(C4C=CC([N+]([O-])=O)=CC=4)=CC4C(=CC=CC=4)N=3)(=O)=[O:21])=[N:12][C:13]3[C:18]([CH:19]=2)=[CH:17][CH:16]=[CH:15][CH:14]=3)=CC=1)([O-])=O.C[N:43]([CH:45]=O)C>C(O)C.[Pd]>[NH2:43][C:45]1[CH:17]=[CH:18][C:13]([S:20]([C:11]2[CH:10]=[CH:19][C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[N:12]=2)=[O:21])=[CH:14][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6228DimethylformamideHCID 867507624-Nitrophenyl-2-quinolylsulfone

생성물 1

HCID 189716682-(4-Aminophenylsulfinyl)quinoline

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

4-Nitrophenyl-2-quinolylsulfone (9.0 mmoles, 2.7 g) was dissolved in 200 ml ethanol and 75 ml DMF and was then hydrogenated over 2.2 g 5% Pd/C at room temperature for 3 hr. The reaction mixture was then filtered through celite and condensed to afford 2-(4-aminophenylsulfinyl)quinoline

후처리

  1. filtrationThe reaction mixture was then filtered through celite and condensed

출처 및 근거

ORD 기록
ord-51004044a14047469e6ace6c8d550860
출처 데이터셋
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05814646

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