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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 330313생성일: 2026년 10월 23일

Water → DL-5 Chloro-6-ethyl-4-[alpha-ethyl-4-(sec-amyloxy)benzyl]aminopyrimidine

https://huagongshe.com/ko/reaction/330313

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물2-BromopentaneHCID 7890—
반응물SodiumHCID 5360545—
반응물DL-5 Chloro-6-ethyl-4-(alphaethyl-4-hydroxybenzylamino)pyrimidineHCID 131716268—
용매TolueneHCID 1140—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물DL-5 Chloro-6-ethyl-4-[alpha-ethyl-4-(sec-amyloxy)benzyl]aminopyrimidineHCID 13171626632.7%

반응 단계

To a solution of 1.1 g of dl-5-chloro-6-ethyl-4-(α-ethyl-4-hydroxybenzyl)aminopyrimidine.sodium salt dissolved in 30 ml of N,N-dimethylformamide was added 0.6 g of 2-bromopentane, and the mixture was stirred at 90° to 100° C. for 8 hours. After completion of the reaction, the reaction mixture was poured into water and separated oily product was extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate and ethyl acetate was distilled off under reduced pressure. The oily product obtained was isolated by column chromatography (Wako Gel C-200, trade name, eluted with toluene:ethyl acetate=7:1) to give 0.4 g of the desired product as pale yellow liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04895849
출처 데이터셋uspto-grants-1990_01
ORD IDord-ef61755fe23349e799366bd7cd7d9630
출처 메모uspto-grants-1990_01