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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77721생성일: 2026년 10월 24일

Hydrochloric Acid → 5-(Trifluoromethyl)pyridin-3-amine

https://huagongshe.com/ko/reaction/77721

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물HydroxylamineHCID 787—
반응물2-Chloro-3-nitro-5-(trifluoromethyl)pyridineHCID 4736950—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물5-(Trifluoromethyl)pyridin-3-amineHCID 140519368%

반응 단계

2-Chloro-3-nitro-5-(trifluoromethyl)pyridine (0.850 g, 3.75 mmol) was dissolved in methanol (17 mL) and palladium on carbon (800 mg of 10%, 50% wet, 0.375 mmol) was added. The mixture was hydrogenated at 60 psi and 20° C. for 16 h. LCMS showed no remaining starting material or hydroxylamine (M+H 213/215, 3:1) intermediate, and showed a mixture of partially reduced product (M+H 163; UVmax 214, 258, & 332 nm) and the fully reduced product (M+H 169; no UV). The mixture was filtered; and the filtrate was rinsed thoroughly, and concentrated in vacuo to give 0.74 g, of the product as the HCl salt. The product was purified by prep HPLC/MS using a 30 mm×100 mm C18 column; 20% CH3CN—H2O (0.1% NH4OH), 1 min, to 40% at 6 min; 60 mL/min; detector set at m/z 163; retention time, 4.4 min. Fractions containing the pure product were combined and concentrated to give an oil, 52 mg, 8% yield. 1H NMR (CDCl3) δ 8.26 (s, 1H); 8.24 (d, 1H); 7.15 (t, 1H); 4.00 (s, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841318B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-678054e7bcd244019686071c0783536f
출처 메모uspto-grants-2014_09