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HRID 1439865생성일: 2026년 10월 26일

2-Aminothiophenol → 2-(4-Fluorophenyl)-2H-1,4-benzothiazin-3(4H)-one

https://huagongshe.com/reaction/1439865

반응식

참여 물질

역할이름HCID투입량
반응물2-AminothiophenolHCID 8713—
반응물Sodium AcetateHCID 517045—
반응물Methyl 2-bromo-2-(4-fluorophenyl)acetateHCID 12717580—
용매EthanolHCID 702—
생성물2-(4-Fluorophenyl)-2H-1,4-benzothiazin-3(4H)-oneHCID 1369076187.6%

반응 단계

To a suspension of 2-aminothiophenol (12.6 g) and sodium acetate (23.6 g) in ethanol (150 ml) is added methyl α-bromo-4-fluorophenylacetate (23.6 g), and the mixture is stirred at room temperature overnight. After the solvent is distilled off, water is added to the residue. The resulting precipitate is separated by filtration, washed, dried, and then recrystallized from tetrahydrofuran-n-hexane to give 2-(4-fluorophenyl)-3-oxo-3,4-dihydro-2H-1,4-benzothiazine (21.7 g) as crystals. M.p. 216°-219° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05496815
출처 데이터셋uspto-grants-1996_03
ORD IDord-5e2a977b30994d0bba62d64549e513b5
출처 메모uspto-grants-1996_03