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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 240271생성일: 2026년 10월 23일

(3R)-3-Aminopiperidine, 3-BOC protected → (R)-tert-butyl 1-(4-(2-cyanobenzyl)-6-methyl-5-oxo-4,5-dihydro-1,2,4-triazin-3-yl)piperidin-3-ylcarbamate

https://huagongshe.com/ko/reaction/240271

반응식

참여 물질

역할이름HCID투입량
반응물(3R)-3-Aminopiperidine, 3-BOC protectedHCID 1514172—
반응물2-((6-methyl-3-(methylthio)-5-oxo-1,2,4-triazin-4(5H)-yl)methyl)benzonitrileHCID 58328534—
생성물(R)-tert-butyl 1-(4-(2-cyanobenzyl)-6-methyl-5-oxo-4,5-dihydro-1,2,4-triazin-3-yl)piperidin-3-ylcarbamateHCID 58328532—

반응 조건

온도130 °C

반응 단계

The mixture of 2-((6-methyl-3-(methylthio)-5-oxo-1,2,4-triazin-4(5H)-yl)methyl)benzonitrile (6, 68 mg, 0.25 mmol) and (R)-tert-butyl piperidin-3-ylcarbamate (60 mg, 0.30 mmol) was ground for 5 min and then heated in a tube under nitrogen atmosphere at 130° C. for 13 h. The mixture was separated by silica gel column, and eluted with 2:1 to 1:1 petroleum ether-ethyl acetate and then with 1:1:2 petroleum ether-dichloromethane-ethyl acetate to give (R)-tert-butyl 1-(4-(2-cyanobenzyl)-6-methyl-5-oxo-4,5-dihydro-1,2,4-triazin-3-yl)piperidin-3-ylcarbamate (7). MS: m/z, 425 (100%, M+1), 447(40%, M+23).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08648073B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-aabb22075e924630b76bc00c261e1e7b
출처 메모uspto-grants-2014_02