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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14513생성일: 2026년 10월 24일

2-Methylpiperidine → 4-(2-Butynyloxy)-5-fluoro-6-(2-methylpiperidino)pyrimidine

https://huagongshe.com/ko/reaction/14513

반응식

참여 물질

역할이름HCID투입량
반응물2-MethylpiperidineHCID 7974—
반응물4-(2-Butynyloxy)-5-fluoro-6-chloropyrimidineHCID 22599717—
용매EthanolHCID 702—
생성물4-(2-Butynyloxy)-5-fluoro-6-(2-methylpiperidino)pyrimidineHCID 5934111571.1%

반응 단계

Into 3 ml of ethanol was resolved 0.3 g of 4-(2-butynyloxy)-6-chloro-5-fluoropyrimidine, 0.45 g of 2-methylpyperidine was added therein, and the mixture was stirred for 5 hours under reflux condition. The reaction mixture was cooled to near room temperature and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.28 g of 4-(2-butynyloxy)-5-fluoro-6-(2-methylpiperidino)pyrimidine (hereinafter, referred to as Compound (1)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732448B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-128a683dc56a4a128028ba8b3f713edc
출처 메모uspto-grants-2010_06