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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43291생성일: 2026년 10월 24일

Triethylamine → 2-fluoro-N-(thiazolo[4,5-c]pyridin-2-yl)-5-(trifluoromethyl)benzamide

https://huagongshe.com/ko/reaction/43291

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Propylphosphonic anhydrideHCID 111923—
반응물2-Fluoro-5-(trifluoromethyl)benzoic acidHCID 688292—
반응물(1,3)Thiazolo(4,5-c)pyridin-2-amineHCID 14252938—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2-fluoro-N-(thiazolo[4,5-c]pyridin-2-yl)-5-(trifluoromethyl)benzamideHCID 8664454072.2%

반응 단계

A mixture of thiazolo[4,5-c]pyridin-2-amine (Milestone Pharm Tech USA Inc.) (1.35 g, 8.93 mmol), 2-fluoro-5-(trifluoromethyl)benzoic acid (2.23 g, 10.72 mmol) and triethylamine (2.71 g, 26.8 mmol) in THF (30 mL) was treated drop wise with 1-propanephosphonic acid cyclic anhydride (50% in ethyl acetate) (6.82 g, 10.72 mmol). The mixture was stirred at room temperature for 12 hrs. The reaction mixture was diluted with EtOAc, and washed with saturated NaHCO3. The organic layer was dried (Na2SO4), filtered, and concentrated. The residue was triturated with Et2O and hexane to afford the title compound (2.2 g, 72%) as a brown solid. 1H NMR (500 MHz, DMSO-d6) δ ppm 7.66 (t, J=9.46 Hz, 1H) 8.07 (m, 1H) 8.12 (d, J=4.88 Hz, 1H) 8.26 (dd, J=6.10, 2.14 Hz, 1H) 8.44 (d, J=5.49 Hz, 1H) 9.07 (s, 1H); MS (DCI/NH3) m/z 342 (M+1)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536336B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-bdacc40749ed429aad131aa32c656c68
출처 메모uspto-grants-2013_09