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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1516381생성일: 2026년 10월 25일

Diisopropylethylamine → 5-Bromo-N-((1SR,2RS)-2-hydroxy-cyclohexyl)-6-(2,2,2-trifluoro-ethoxy)-nicotinamide

https://huagongshe.com/reaction/1516381

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물2-Aminocyclohexanol hydrochlorideHCID 21877202—
반응물5-Bromo-6-(2,2,2-trifluoroethoxy)-3-pyridinecarboxylic acidHCID 58192592—
용매DimethylformamideHCID 6228—
생성물5-Bromo-N-((1SR,2RS)-2-hydroxy-cyclohexyl)-6-(2,2,2-trifluoro-ethoxy)-nicotinamideHCID 5819259181.7%

반응 단계

5-Bromo-6-(2,2,2-trifluoro-ethoxy)-nicotinic acid (75.0 g, 0.25 mol) was dissolved in DMF (850 mL). To the solution was added TBTU (91.0 g, 0.275 mol), N,N-diisopropylethyl amine (214 mL, 1.25 mol) and (1SR,2RS)-2-amino-cyclohexanol hydrochloride (41.7 g, 0.275 mol). The reaction mixture was stirred for 1.5 h at room temperature. The solvent was evaporated in vacuo, the residue was partitioned between ethyl acetate (2500 mL) and 1 N sodium hydroxide solution (2000 mL), the water phase was separated, extracted once more with ethyl acetate (1000 mL) and the organic phases were washed 2 times with water (2×1500 mL). Organic phases were pooled, dried with MgSO4 and concentrated to about 900 mL. The product precipitated upon stirring and cooling to 0° C. Filtration, washing with ethyl acetate/n-heptane (1:1) and drying in vacuo gave the title compound (81.1 g) as a white solid; MS (ISP) 397, 399 (M)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08227491B2
출처 데이터셋uspto-grants-2012_07
ORD IDord-74a4fb52365c421cb426c6bba343c669
출처 메모uspto-grants-2012_07