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Benzene, 2-fluoro-4-methyl-1-nitro- → 6-Fluoro-2-(5-methyl-2-nitroanilino)benzo[b]thiophene-3-carbonitrile

HRID 1281815
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HRID 1281815 반응식
[NH2:1][C:2]1[S:6][C:5]2[CH:7]=[C:8]([F:11])[CH:9]=[CH:10][C:4]=2[C:3]=1[C:12]#[N:13].F[C:15]1[CH:16]=[C:17]([CH3:24])[CH:18]=[CH:19][C:20]=1[N+:21]([O-:23])=[O:22]>CS(C)=O>[F:11][C:8]1[CH:9]=[CH:10][C:4]2[C:3]([C:12]#[N:13])=[C:2]([NH:1][C:15]3[CH:16]=[C:17]([CH3:24])[CH:18]=[CH:19][C:20]=3[N+:21]([O-:23])=[O:22])[S:6][C:5]=2[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 67966Benzene, 2-fluoro-4-methyl-1-nitro-HCID 184221842-Amino-6-fluorobenzo[b]thiophene-3-carbonitrile

생성물 1

HCID 184222356-Fluoro-2-(5-methyl-2-nitroanilino)benzo[b]thiophene-3-carbonitrile수율 88.1%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

In the same manner as in Starting Material Synthesis Example 51 and using 2-amino-6-fluorobenzo[b]thiophene-3-carbonitrile (5.0 g), 3-fluoro-4-nitrotoluene (4.7 g) and dimethyl sulfoxide (55 ml), 6-fluoro-2-(5-methyl-2-nitroanilino)benzo[b]thiophene-3-carbonitrile (7.5 g) was obtained.

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후처리

  1. customMaterial Synthesis Example 51

출처 및 근거

ORD 기록
ord-78a8c42e08214c1c8cc1585b38597dea
출처 데이터셋
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06455521B1

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