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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14522생성일: 2026년 10월 24일

3,5-Dimethylpiperidine → 4-(3,5-Dimethylpiperidino)-5-fluoro-6-(2-pentynyloxy)pyrimidine

https://huagongshe.com/ko/reaction/14522

반응식

참여 물질

역할이름HCID투입량
반응물3,5-DimethylpiperidineHCID 118259—
반응물4-Chloro-5-fluoro-6-(2-pentynyloxy)pyrimidineHCID 59341120—
생성물4-(3,5-Dimethylpiperidino)-5-fluoro-6-(2-pentynyloxy)pyrimidineHCID 5782468584.7%

반응 단계

0.2 g of 4-chloro-5-fluoro-6-(2-pentynyloxy)pyrimidine and 0.32 g of 3,5-dimethylpiperidine (cis/trans=about 3/1) were mixed and left for 3 hours at room temperature. The reaction mixture was subjected to silica gel column chromatography to obtain 0.23 g of 4-(3,5-dimethylpiperidino)-5-fluoro-6-(2-pentynyloxy)pyrimidine (hereinafter, referred to as Compound (11)). Compound (11) had the cis/trans diastereomer originated two methyls on the piperidine ring. The ratio of the cis/trans diastereomer was about 3.8/1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732448B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-359178bc0bbb4b3da86334cd14e4f2bb
출처 메모uspto-grants-2010_06