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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33464생성일: 2026년 10월 24일

Pyridine → N-(2-(piperidin-1-yl)phenyl)isoxazole-5-carboxamide

https://huagongshe.com/ko/reaction/33464

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물2-(Piperidin-1-yl)anilineHCID 458795—
반응물Isoxazole-5-carbonyl chlorideHCID 2736707—
반응물HOBt resinHCID 16217185—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물N-(2-(piperidin-1-yl)phenyl)isoxazole-5-carboxamideHCID 11277266100%

반응 단계

To PS-HOBt resin (0.1 mmol) was added anhydrous dichloromethane (“DCM”) (1 mL) followed by pyridine (0.5 mmol) and isoxazole-5-carbonyl chloride (Lancaster) (0.3 mmol). The mixture was shaken at room temperature for 3 h and was then filtered. The resin was washed successively with tetrahydrofuran (“THF”) (3×) and DCM (3×) and dried in vacuo. To this acylated resin was added a solution of 2-piperidinoaniline (Lancaster) (0.05 mmol, 0.5 eq) in anhydrous THF (1 mL) and the mixture was shaken at room temperature for 16 h. The mixtue was then filtered and the resin washed with THF and DCM as described above. The combined filtrate and washings were concentrated under reduced pressure to yield the product. Yield: 100%. MS: 272 (M+1). LC/MS purity: 100%. 1HNMR (CDCl3, 300 MHz): δ 8.2 (d, 1H), 7.85 (t, 2H), 7.55 (m, 1H), 7.4 (m, 2H), 3.8-3.2 (bm, 4H), 2.7-1.9 (bm, 4H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429603B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-cc1fc177866d45a0b0846b9269bdeffc
출처 메모uspto-grants-2008_09