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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 620165생성일: 2026년 10월 25일

Piperidine → 4-Methoxymethyl-5-methyl-6-piperidinopyrimidine

https://huagongshe.com/reaction/620165

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물4-Methoxymethyl-5-methyl-6-chloropyrimidineHCID 14306160—
용매TetrahydrofuranHCID 8028—
생성물4-Methoxymethyl-5-methyl-6-piperidinopyrimidineHCID 14306161—

반응 단계

Piperidine (15 ml) in tetrahydrofuran (40 ml) was added dropwise to a solution of 4-methoxymethyl-5-methyl-6-chloropyrimidine (5 g) in tetrahydrofuran (40 ml). The mixture was heated under reflux for 7 hours and then allowed to stand overnight at room temperature. It was filtered, stripped, and water added to the residual oil. The pH was lowered to 7.5 (HCl) and extracted with chloroform. Extracts were dried (K2CO3) and stripped to give 4-methoxymethyl-5-methyl-6-piperidinopyrimidine, 6.08 g, as an oil, which solidified on cooling to 5° (m.p. 45°-47°). It was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04820708
출처 데이터셋uspto-grants-1989_04
ORD IDord-b1d7a3f1eb314a25bbe67e553b010679
출처 메모uspto-grants-1989_04