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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72885생성일: 2026년 10월 24일

Diisopropylethylamine → Tert-butyl 4-[[benzyl-[2-oxo-2-(2-pyridyl)ethyl]amino]methyl]-4-hydroxy-piperidine-1-carboxylate

https://huagongshe.com/ko/reaction/72885

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물2-Bromo-1-(2-pyridinyl)-1-ethanone hydrobromideHCID 2776231—
반응물Tert-butyl 4-((benzylamino)methyl)-4-hydroxypiperidine-1-carboxylateHCID 68291338—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물Tert-butyl 4-[[benzyl-[2-oxo-2-(2-pyridyl)ethyl]amino]methyl]-4-hydroxy-piperidine-1-carboxylateHCID 6829142392%

반응 단계

To tert-butyl 4-[(benzylamino)methyl]-4-hydroxy-piperidine-1-carboxylate (3.0 g, 9.36 mmol) in DMF (19 mL) at 0° C. was added diisopropyl ethylamine (3.4 mL, 19.66 mmol) followed by the addition of 2-bromo-1-(2-pyridyl)ethanone hydrobromide salt (2.6 g, 9.36 mmol) and reaction mixture was stirred for 2 hours warming from 0° C. to 10° C. The reaction mixture was diluted with ethyl acetate and washed with sat. NaHCO3 solution and then brine. The organics were separated, dried over Na2SO4, filtered and concentrated in vacuo to give a residue, which was purified using silica gel column chromatography using MeOH/DCM (1-15%) as eluent to give tert-butyl 4-[[benzyl-[2-oxo-2-(2-pyridyl)ethyl]amino]methyl]-4-hydroxy-piperidine-1-carboxylate (3.8, 92%). ESI-MS m/z calc. 439.2. Found 440.0 (M+1)+; Retention time: 1.12 minutes (3 min run).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828996B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-95922c8713b64476bfe983225eb4b428
출처 메모uspto-grants-2014_09