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5'-fluoro-N-methyl-2'-methylsulphonylacetylformanilide → Flosequinoxan

HRID 1085908
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인쇄 미리보기

반응식

HRID 1085908 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]([C:12](=[O:18])[CH2:13][S:14]([CH3:17])(=[O:16])=[O:15])=[C:6]([CH:11]=1)[N:7]([CH3:10])[CH:8]=O>COCCO>[F:1][C:2]1[CH:11]=[C:6]2[C:5]([C:12](=[O:18])[C:13]([S:14]([CH3:17])(=[O:16])=[O:15])=[CH:8][N:7]2[CH3:10])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 867447425'-fluoro-N-methyl-2'-methylsulphonylacetylformanilide

생성물 1

HCID 131270Flosequinoxan

시약·촉매·용매 1

HCID 80192-Methoxyethanol용매

실험 절차

A solution of 5'-fluoro-N-methyl-2'-methylsulphonylacetylformanilide (0.20 g), prepared in a similar manner to that described in Example 11, in 2-methoxyethanol (25 ml) was heated at 97° for 5.3 hours. The mixture was allowed to cool to ambient temperature and then evaporated in vacuo to give 7-fluoro-1-methyl-3-methylsulphonyl-4-quinolone, m.p. 234°-235° (0.19 g).

후처리

  1. temperaturewas heated at 97° for 5.3 hours
  2. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-8a0f7eaa1a7143279601b127031ddeb0
출처 데이터셋
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05011931

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