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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 550864생성일: 2026년 10월 24일

Picolinic acid → Pyridine-2-carboxylic acid (3-hydroxy-adamantan-1-yl)-amide

https://huagongshe.com/ko/reaction/550864

반응식

참여 물질

역할이름HCID투입량
반응물Picolinic acidHCID 1018—
반응물TriethylamineHCID 8471—
반응물3-Amino-1-adamantanolHCID 658645—
반응물Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
용매DimethylformamideHCID 6228—
생성물Pyridine-2-carboxylic acid (3-hydroxy-adamantan-1-yl)-amideHCID 5916106897%

반응 단계

To a 40 ml vial was added picolinic acid (0.68 g, 5.5 mmol), DMF (15 ml), triethylamine (0.90 mL, 6.4 mmol), and O-(Benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HBTU, 2.3 g, 6.0 mmol). The mixture was stirred at rt for 5 minutes to get a clear solution. 3-Amino-adamantanol (0.84 g, 5.0 mmol; AK Scientific, 897-4G Independence Ave., Mountain View, Calif. 94043) was added to the above solution and stirred at rt for 2 hours. DMF was removed in Genevac and the residue was dissolved in DCM (20 mL), washed with 1N aqueous NaOH, water and brine, dried over Na2SO4 and concentrated under reduced pressure to afford 1.32 g (97%) of crude title compound, pyridine-2-carboxylic acid (3-hydroxy-adamantan-1-yl)-amide, as an oil, which became a colorless solid upon standing at room temperature. LC/MS (Gradient: acetonitrile in water, 20-85%, in 1.7 minutes with a cycle time of 2 min. Flow rate: 5.0 mL/min. Mobile phase additive: 30 mM of ammonium formate. Column: Inertsil® ODS-3, 50×4.6 mm, 3 μm particle size (GL Sciences, Tokyo, Japan)): Retention time: 0.79 min; purity (UV254): 100%; ESI-MS m/z: 273 (M+H)+. It was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07947680B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-5fb38220987a452f8e35afd995c24ff3
출처 메모uspto-grants-2011_05