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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 499272생성일: 2026년 10월 25일

Pyridine-2-carbonitrile → 6-Fluoro-2-(2-pyridyl)-4H-1,3-benzothiazine-4-one

https://huagongshe.com/reaction/499272

반응식

참여 물질

역할이름HCID투입량
반응물Pyridine-2-carbonitrileHCID 7522—
반응물5-Fluoro-2-mercaptobenzoic acidHCID 2783371—
용매PyridineHCID 1049—
생성물6-Fluoro-2-(2-pyridyl)-4H-1,3-benzothiazine-4-oneHCID 597504774%

반응 조건

온도135 °C

반응 단계

A mixture of 5-fluoro-2-mercaptobenzoic acid (1.50 g, 8.7 mmol), 2-cyanopyridine (0.92 g, 8.8 mmol) and pyridine (30.0 ml) was refluxed at 135° C. for 48 hrs as described in Example 9. The reaction mixture was concentrated. The residue was subjected to a silica gel column chromatography and eluted with hexane-ethyl acetate (2:1, v/v). The resultant product was recrystallized from ethanol to give the titled compound (0.09 g, 4%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07767665B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-887478f8a4ea48acbb100b857cb5eafb
출처 메모uspto-grants-2010_08