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1-(Trifluoromethylcarbonylaminosulphonyl)-3-nitrobenzene → 1-(Trifiuoromethyl carbonylaminosulphonyl)-3-aminobenzene

HRID 2379332
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인쇄 미리보기

반응식

HRID 2379332 반응식
[F:1][C:2]([F:19])([F:18])[C:3]([NH:5][S:6]([C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([N+:15]([O-])=O)[CH:10]=1)(=[O:8])=[O:7])=[O:4]>[Pd].O.C(O)C>[F:19][C:2]([F:1])([F:18])[C:3]([NH:5][S:6]([C:9]1[CH:14]=[CH:13][CH:12]=[C:11]([NH2:15])[CH:10]=1)(=[O:7])=[O:8])=[O:4]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 189577841-(Trifluoromethylcarbonylaminosulphonyl)-3-nitrobenzene

생성물 1

HCID 217455061-(Trifiuoromethyl carbonylaminosulphonyl)-3-aminobenzene수율 70%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 702Ethanol용매HCID 962Water용매

실험 절차

In the same way as that described in Example 11, Step 2, using 1-(trifluoromethylcarbonylaminosulphonyl)-3-nitrobenzene (2.7 g, 9.1 mmol), 10% palladium on carbon (0.25 g, 9% (w/w)) in water (3 ml) and ethanol (70 ml), the title compound (1.7 g, 70%) was afforded as a colourless solid. mp 106°-108° C. 1H NMR (360 MHz, D6 -DMSO) δ 6.59 (1H, m), 6.88 (1H, m), 7.02 (2H, m).

출처 및 근거

ORD 기록
ord-3c6bb15660594b0b8bc84f15131448e1
출처 데이터셋
uspto-grants-1994_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05360802

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