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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 930182생성일: 2026년 10월 25일

4,4-Dimethylpiperidine → 5-(3'-Amino-4,4-dimethyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-6'-yl)-1,3-dimethyl-tetrahydro-pyrimidin-2-one

https://huagongshe.com/reaction/930182

반응식

참여 물질

역할이름HCID투입량
반응물4,4-DimethylpiperidineHCID 138100—
반응물[2-Bromo-6-(1,3-dimethyl-2-oxo-hexahydro-pyrimidin-5-yl)-pyridin-3-yl]-carbamic acid tert-butyl esterHCID 59771238—
생성물5-(3'-Amino-4,4-dimethyl-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-6'-yl)-1,3-dimethyl-tetrahydro-pyrimidin-2-oneHCID 59771237—

반응 단계

The title compound is prepared from [2-bromo-6-(1,3-dimethyl-2-oxo-hexahydro-pyrimidin-5-yl)-pyridin-3-yl]-carbamic acid tert-butyl ester (as prepared in the previous step) and 4,4-dimethylpiperidine (US 2003236247) following the literature procedure of Buchwald (Org. Lett., 4, 2885-8 (2002)). The residue obtained is purified by silica gel chromatography with an appropriate solvent mixture. After isolation, removal of the BOC protecting group from the resulting intermediate is carried out by stirring at RT in TFA-DCM (1:2), monitoring by TLC for completion, and then concentration in vacuo.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09296726B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-e7e9298bc54d43309a1bc2fcbcff7f2d
출처 메모uspto-grants-2016_03