Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 384698생성일: 2026년 10월 25일
Triethylamine → Benzyl 4-((5-bromo-2-pivalamidopyridin-4-ylamino)methyl)piperidine-1-carboxylate
https://huagongshe.com/reaction/384698
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-Aminomethyl-1-N-Cbz-piperidine | HCID 21955499 | — |
| 반응물 | N-(5-bromo-4-chloropyridin-2-yl)-2,2-dimethylpropanamide | HCID 59613421 | — |
| 용매 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 생성물 | Benzyl 4-((5-bromo-2-pivalamidopyridin-4-ylamino)methyl)piperidine-1-carboxylate | HCID 59613492 | 87.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08367658B2 |
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| 출처 데이터셋 | uspto-grants-2013_02 |
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| ORD ID | ord-a00b10751029486d80d9e3dfdd8c6e3b |
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| 출처 메모 | uspto-grants-2013_02 |
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