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Triethylamine → Flosequinoxan

HRID 1085914
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인쇄 미리보기

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HRID 1085914 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.C(N(CC)CC)C>CCCCCC>[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

4

반응물 2

HCID 8471TriethylamineHCID 867447425'-fluoro-N-methyl-2'-methylsulphonylacetylformanilide

생성물 1

HCID 131270Flosequinoxan

시약·촉매·용매 1

HCID 8058Hexane용매

실험 절차

A mixture of 5'-fluoro-N-methyl-2'-methylsulphonylacetylformanilide (0.20 g), prepared in a similar manner to that described in Example 11, and triethylamine (20 ml) was stirred at ambient temperature for 2.5 hours. Hexane (30 ml) was added to the mixture. The solid product collected by filtration of the mixture was washed with hexane (2×5 ml) and dried at 50° in vacuo to give 7-fluoro-1-methyl-3-methylsulphonyl-4-quinolone, m.p. 233°-234.5° (0.16 g).

후처리

  1. customprepared in a similar manner to that
  2. filtrationThe solid product collected by filtration of the mixture
  3. washwas washed with hexane (2×5 ml)
  4. customdried at 50° in vacuo

출처 및 근거

ORD 기록
ord-b9cd02beca144f6398ac4b82babe2a90
출처 데이터셋
uspto-grants-1991_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05011931

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