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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Amino-1-Boc-piperidine | HCID 1268291 | — |
| 반응물 | 5-(Benzyloxy)-2-chloropyridine | HCID 10013717 | — |
| 반응물 | HCID 178418922 | HCID 178418922 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 촉매 | Binap, (A+-)- | HCID 634876 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 4-(5-Benzyloxy-pyridin-2-ylamino)-piperidine-1-carboxylic acid tert-butyl ester | HCID 67400770 | 87% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08026255B2 |
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| 출처 데이터셋 | uspto-grants-2011_09 |
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| ORD ID | ord-ab6421cf164e4204894db637ac51dfa3 |
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| 출처 메모 | uspto-grants-2011_09 |
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