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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 337497생성일: 2026년 10월 24일

Water → N-[4-(2-Furyl)-5-(tetrahydropyran-4-ylcarbonyl)thiazol-2-yl]-2-(trifluoromethoxy)benzamide

https://huagongshe.com/ko/reaction/337497

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-(Trifluoromethoxy)benzoyl ChlorideHCID 2777241—
반응물2-Amino-4-(2-furyl)-5-(tetrahydropyran-4-ylcarbonyl)thiazoleHCID 86612468—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매PyridineHCID 1049—
생성물N-[4-(2-Furyl)-5-(tetrahydropyran-4-ylcarbonyl)thiazol-2-yl]-2-(trifluoromethoxy)benzamideHCID 2314420853%

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온도80 °C

반응 단계

Compound 454 (125 mg, 0.450 mmol) and DMAP (0.022 mmol) were suspended in pyridine (2 mL), and 2-(trifluoromethoxy)benzoyl chloride (202 mg, 0.900 mmol) was added thereto, followed by stirring at 80° C. for 6 hours. The reaction mixture was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, and then the solvent was distilled away under reduced pressure. The resulting residue was recrystallized from ethanol to afford the entitled Compound 475 (111 mg, 53%) as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889718B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-aa3505459a4e4d738412fa136f04b93c
출처 메모uspto-grants-2014_11