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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 913151생성일: 2026년 10월 24일

4-Amino-1-Boc-piperidine → 4-(5-Benzyloxy-pyridin-2-ylamino)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/913151

반응식

참여 물질

역할이름HCID투입량
반응물4-Amino-1-Boc-piperidineHCID 1268291—
반응물5-(Benzyloxy)-2-chloropyridineHCID 10013717—
반응물HCID 178418922HCID 178418922—
촉매palladium(II) acetateHCID 167845—
촉매Binap, (A+-)-HCID 634876—
용매TolueneHCID 1140—
생성물4-(5-Benzyloxy-pyridin-2-ylamino)-piperidine-1-carboxylic acid tert-butyl esterHCID 6740077087%

반응 조건

온도70 °C

반응 단계

A stirred suspension of 5-benzyloxy-2-chloro-pyridine (12.4 g, 56.4 mmol, 1.0 equiv; prepared as described in WO 9728 128 A1 (Zeneca Ltd., UK)), 4-amino-piperidine-1-carboxylic acid tert-butyl ester (11.31 g, 56.4 mmol, 1.0 equiv), palladium(II) acetate (0.51 g, 2.3 mmol, 0.04 equiv) and rac-2,2′-bis(diphenylphosphino)-1,1′-binaphthalene (1.44 g, 2.3 mmol, 0.04 equiv) in toluene (250 mL) was treated at rt with KOtert-Bu (6.71 g, 67.7 mmol, 1.2 equiv) and subsequently warmed to 70° C. After 7 h, the reaction mixture was poured into crashed ice and filtered over dicalite and extracted twice with toluene. The combined organic layers were dried over MgSO4, filtered and concentrated by evaporation under reduced pressure. The crude product was purified by column chromatography on silica eluting with a gradient of dichloromethane/methanol to give 18.73 g (87%) of the title compound as a light yellow solid. MS (ISP): 384.1 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08026255B2
출처 데이터셋uspto-grants-2011_09
ORD IDord-ab6421cf164e4204894db637ac51dfa3
출처 메모uspto-grants-2011_09