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HRID 330313作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物2-BromopentaneHCID 7890—
反応物SodiumHCID 5360545—
反応物DL-5 Chloro-6-ethyl-4-(alphaethyl-4-hydroxybenzylamino)pyrimidineHCID 131716268—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物DL-5 Chloro-6-ethyl-4-[alpha-ethyl-4-(sec-amyloxy)benzyl]aminopyrimidineHCID 13171626632.7%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04895849
出典データセットuspto-grants-1990_01
ORD IDord-ef61755fe23349e799366bd7cd7d9630
出典メモuspto-grants-1990_01