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2,4-Difluoronitrobenzene → Ethyl 6-bromo-2-(5-fluoro-2-nitroanilino)benzo[b]thiophene-3-carboxylate

HRID 649907
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HRID 649907 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[C:9]([C:10]([O:12][CH2:13][CH3:14])=[O:11])=[C:8]([NH2:15])[S:7][C:6]=2[CH:16]=1.F[C:18]1[CH:23]=[C:22]([F:24])[CH:21]=[CH:20][C:19]=1[N+:25]([O-:27])=[O:26]>CS(C)=O>[Br:1][C:2]1[CH:3]=[CH:4][C:5]2[C:9]([C:10]([O:12][CH2:13][CH3:14])=[O:11])=[C:8]([NH:15][C:18]3[CH:23]=[C:22]([F:24])[CH:21]=[CH:20][C:19]=3[N+:25]([O-:27])=[O:26])[S:7][C:6]=2[CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 679672,4-DifluoronitrobenzeneHCID 18422163Ethyl 6-bromo-2-aminobenzo[b]thiophene-3-carboxylate

생성물 1

HCID 18422148Ethyl 6-bromo-2-(5-fluoro-2-nitroanilino)benzo[b]thiophene-3-carboxylate수율 77.7%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

In the same manner as in Starting Material Synthesis Example 4 and using ethyl 6-bromo-2-aminobenzo[b]thiophene-3-carboxylate (8.8 g), 2,4-difluoronitrobenzene (5.6 g) and dimethyl sulfoxide (100 ml), ethyl 6-bromo-2-(5-fluoro-2-nitroanilino)benzo[b]thiophene-3-carboxylate (10 g) was obtained.

후처리

  1. customMaterial Synthesis Example 4

출처 및 근거

ORD 기록
ord-9af5125668ec4ac58507b58c180803fd
출처 데이터셋
uspto-grants-2001_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06271225B1

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