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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 556859생성일: 2026년 10월 26일

Triethylamine → Benzyl 4-((5-bromo-2-pivalamidopyridin-4-ylamino)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/556859

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-Aminomethyl-1-N-Cbz-piperidineHCID 21955499—
반응물N-(5-bromo-4-chloropyridin-2-yl)-2,2-dimethylpropanamideHCID 59613421—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물Benzyl 4-((5-bromo-2-pivalamidopyridin-4-ylamino)methyl)piperidine-1-carboxylateHCID 5961349287.2%

반응 조건

온도210 °C

반응 단계

Two capped microwave reaction vials each containing a solution of N-(5-bromo-4-chloropyridin-2-yl)pivalamide (0.55 g, 1.89 mmol), benzyl 4-(aminomethyl)piperidine-1-carboxylate (1.07 g, 2 eq.) and triethylamine (0.80 mL, 3 eq.) in NMP (3.8 mL) were heated at 210° C. by microwave irradiation for 1.5 hr and then allowed to cool. The contents of the two vials were combined and partitioned between EtOAc (15 mL) and sat. NaHCO3 (150 mL). The organic layer was retained whilst the aqueous was further extracted with EtOAc (15 mL). The organic extracts were combined, washed with brine (50 mL), dried (MgSO4) and concentrated. The crude material was purified by chromatography on a 40+M Biotage silica column, eluting with a gradient of EtOAc in dichloromethane, to give the title compound as a clear oil (0.83 g, 43%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08058045B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-90a6831844ba4adda8508b0b6e7e7f3c
출처 메모uspto-grants-2011_11