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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72466생성일: 2026년 10월 26일

3-(Trifluoromethyl)aniline → 5-Chloro-2-(3-((3-(trifluoromethyl)phenyl)amino)azetidin-1-yl)nicotinic acid

https://huagongshe.com/reaction/72466

반응식

참여 물질

역할이름HCID투입량
반응물3-(Trifluoromethyl)anilineHCID 7375—
반응물Potassium CarbonateHCID 11430—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물Methyl 5-chloro-2-(3-((methylsulfonyl)oxy)azetidin-1-yl)nicotinateHCID 86697874—
용매AcetonitrileHCID 6342—
생성물5-Chloro-2-(3-((3-(trifluoromethyl)phenyl)amino)azetidin-1-yl)nicotinic acidHCID 6795834636%

반응 조건

온도160 °C

반응 단계

To a solution of 3-(Trifluoromethyl)aniline (0.047 ml, 0.374 mmol) in acetonitrile (0.5 ml), potassium carbonate (67.21 mg, 0.486 mmol) was added followed by the addition of methyl 5-chloro-2-(3-((methylsulfonyl)oxy)azetidin-1-yl)nicotinate (D63)(120 mg, 0.374 mmol). The reaction mixture was heated at 160° C. under microwave irradiation for 25 min. Lithium hydroxide monohydrate (23.54 mg, 0.561 mmol) was added and the resulting reaction mixture was heated at 150° C. under microwave irradiation for 5 min. Solvents were evaporated in vacuo and the residue was diluted with water (5 ml) and HCl 1M (15 ml) and extracted with ethyl acetate (3×20 ml). Collected organics, after solvent evaporation, afforded the title compound (D115) (50 mg)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828987B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-ac4769fab979437ea79adf759b8ebaaa
출처 메모uspto-grants-2014_09