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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 395생성일: 2026년 10월 23일

Piperidine → Tert-butyl 6-piperidin-1-ylpyridine-3-carboxylate

https://huagongshe.com/ko/reaction/395

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물(tert-Butyl) 6-bromonicotinateHCID 26369925—
시약Cesium carbonateHCID 10796—
촉매Binap, (A+-)-HCID 634876—
촉매Palladium (II) acetateHCID 4144353—
용매1,4-DioxaneHCID 31275—
생성물Tert-butyl 6-piperidin-1-ylpyridine-3-carboxylateHCID 9150937561.94%

반응 조건

온도80 °C

반응 단계

In a 100 mL round-bottomed flask was tert-butyl 6-bromonicotinate (516 mg, 2 mmol), piperidine (237 µl, 2.40 mmol), and CESIUM CARBONATE (977 mg, 3.00 mmol) in dioxane (9763 µl) to give a white suspension. The solution was degassed with N2 (g) fo 20 mins. PALLADIUM(II) ACETATE (22.45 mg, 0.10 mmol) and BINAP (62.3 mg, 0.10 mmol) were added under N2 (g) and the reaction was heated to 100 °C. Start Time: 01-Jul-10 1:10:32 PM -0400. The reaction was checked by LC-MS (complete), filtered, rinsed with DCM, concentrated in vacuo. _02 July 2010_ Purification by Iscos (25 g) using 100% Hexanes -> 50% EtOAc in Hexanes afforded a white solid. 325 mg obtained. 1H NMR (300 MHz, DMSO- _d_ 6) d ppm 1.51 - 1.57 (m, 12 H) 1.57 - 1.77 (m, 5 H) 3.58 - 3.74 (m, 4 H) 6.78 - 6.92 (m, 1 H) 7.88 (dd, _J_ =9.16, 2.36 Hz, 1 H) 8.60 (dd, _J_ =2.45, 0.57 Hz, 1 H). LC-MS: Rt = 2.37 min. Method: Short Purity. MS ES+: 263.2 [M+H]+.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-b099625680284510ba7d7318538524ab
출처 메모750 AstraZeneca ELN dataset