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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 337728생성일: 2026년 10월 24일

Piperidine → N-(2,4-Dimethoxybenzyl)pyrimidin-4-amine

https://huagongshe.com/ko/reaction/337728

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물4-AminopyrimidineHCID 68958—
반응물2,4-DimethoxybenzaldehydeHCID 69175—
반응물Sodium borohydrideHCID 4311764—
용매WaterHCID 962—
용매TolueneHCID 1140—
생성물N-(2,4-Dimethoxybenzyl)pyrimidin-4-amineHCID 6336299552.4%

반응 단계

A solution of 4-aminopyrimidine (20.0 g, 210 mmol), 2,4-dimethoxybenzaldehyde (69.9 g, 421 mmol) and piperidine (2.08 mL, 21.0 mmol) in toluene (1 L) was stirred for 7 hours under reflux, and the solvent was subjected to azeotropic distillation with water. After allowing to cool, the reaction solution was diluted with ethanol (500 mL). Sodium borohydride (7.96 g, 210 mmol) was added thereto with cooling on ice, and the mixture was stirred at room temperature for 16 hours. To the reaction solution, water (500 mL) was added, and an organic layer was extracted. The thus obtained organic layer was dried over anhydrous sodium sulfate. After vacuum concentration, the residue was purified with silica gel chromatography (ethyl acetate/methanol=95:5) to yield the title compound (27.0 g, 52%) as a colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889741B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-9da8027bd5b44ede81a610d6f916a157
출처 메모uspto-grants-2014_11