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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 240742생성일: 2026년 10월 25일

Hydrochloric Acid → 5-(4-Cyano-phenyl)-N-(4-hydroxy-piperidin-1-yl)-6-(2,2,2-trifluoro-ethoxy)-nicotinamide

https://huagongshe.com/reaction/240742

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DiisopropylethylamineHCID 81531—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물1-Aminopiperidin-4-OLHCID 12125645—
반응물5-(4-Cyanophenyl)-6-(2,2,2-trifluoroethoxy)nicotinic acidHCID 66678700—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물5-(4-Cyano-phenyl)-N-(4-hydroxy-piperidin-1-yl)-6-(2,2,2-trifluoro-ethoxy)-nicotinamideHCID 71293983—

반응 단계

In a 5 mL round-bottomed flask, the above prepared 5-(4-cyano-phenyl)-6-(2,2,2-trifluoro-ethoxy)-nicotinic acid (0.050 g, 155 μmol, Eq: 1.00) was combined with THF (1 mL) and DMF (1 mL) to give a colorless solution. TBTU (74.7 mg, 233 μmol, Eq: 1.5) and N,N-diisopropyl-ethylamine (100 mg, 135 μL, 776 μmol, Eq: 5) were added. The reaction mixture was stirred for 10 min at RT, then 1-aminopiperidin-4-ol (21.6 mg, 186 μmol, Eq: 1.2, CAN 79414-82-7) was added and the reaction mixture kept at RT overnight. Pouring into 25 mL 1 M HCl, extraction with EtOAc (2×50 mL), washing with 1 M NaOH, drying over Na2SO4 and evaporation of all solvents in vacuo, followed by stirring for 15 min with 3 mL of heptane containing 3 drops of EtOAc, generated 51 mg of the title compound as white solid; MS (EI) 421.1 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08648099B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-c8360572b7914669bfa75517d570e585
출처 메모uspto-grants-2014_02