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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 524114생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/524114

반응식

참여 물질

역할이름HCID투입량
반응물(3R)-3-Aminopiperidine, 3-BOC protectedHCID 1514172—
반응물4-(2-bromo-5-fluorobenzyl)-6-methyl-3-(methylthio)-1,2,4-triazin-5(4H)-oneHCID 58328530—
생성물(R)-tert-butyl 1-(4-(2-bromo-5-fluorobenzyl)-6-methyl-5-oxo-4,5-dihydro-1,2,4-triazin-3-yl)piperidin-3-ylcarbamateHCID 58328539—

반응 조건

온도135 °C

반응 단계

The mixture of 4-(2-bromo-5-fluorobenzyl)-6-methyl-3-(methylthio)-1,2,4-triazin-5(4H)-one (17, 180 mg, 0.523 mmol) and (R)-tert-butyl piperidin-3-ylcarbamate (208 mg, 1.04 mmol) was ground for 5 min and then heated in a tube under nitrogen atmosphere at 135° C. for 13 h. The mixture was separated by silica gel column, and eluted with 10-50% ethyl acetate in petroleum ether to give (R)-tert-butyl 1-(4-(2-bromo-5-fluorobenzyl)-6-methyl-5-oxo-4,5-dihydro-1,2,4-triazin-3-yl)piperidin-3-ylcarbamate (18). MS: m/z, 496 (100%, M+1), 498 (100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09340523B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-06b47f36ca5646669d554d5503cd90d5
출처 메모uspto-grants-2016_05