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Ethyl 2-amino-1-benzothiophene-3-carboxylate → Ethyl 2-(5-bromo-2-nitroanilino)benzo[b]thiophene-3-carboxylate

HRID 1281756
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인쇄 미리보기

반응식

HRID 1281756 반응식
[NH2:1][C:2]1[S:6][C:5]2[CH:7]=[CH:8][CH:9]=[CH:10][C:4]=2[C:3]=1[C:11]([O:13][CH2:14][CH3:15])=[O:12].Br[C:17]1[CH:22]=[C:21]([Br:23])[CH:20]=[CH:19][C:18]=1[N+:24]([O-:26])=[O:25]>CS(C)=O>[Br:23][C:21]1[CH:20]=[CH:19][C:18]([N+:24]([O-:26])=[O:25])=[C:17]([CH:22]=1)[NH:1][C:2]1[S:6][C:5]2[CH:7]=[CH:8][CH:9]=[CH:10][C:4]=2[C:3]=1[C:11]([O:13][CH2:14][CH3:15])=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 699464Ethyl 2-amino-1-benzothiophene-3-carboxylateHCID 123156462,4-Dibromo-1-nitrobenzene

생성물 1

HCID 18422260Ethyl 2-(5-bromo-2-nitroanilino)benzo[b]thiophene-3-carboxylate

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

In the same manner as in Starting Material Synthesis Example 4 and using ethyl 2-aminobenzo[b]thiophene-3-carboxylate, 2,4-dibromonitrobenzene and dimethyl sulfoxide, ethyl 2-(5-bromo-2-nitroanilino)benzo[b]thiophene-3-carboxylate is obtained.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customMaterial Synthesis Example 4
  • 출처 및 근거

    ORD 기록
    ord-42bac867a8f0486a9bfb22686973e25a
    출처 데이터셋
    uspto-grants-2002_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06455521B1

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