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HRID 4514생성일: 2026년 10월 24일

Potassium Carbonate → 3-Chloro-4-[(5-chloropyrimidin-2-yl)oxy]aniline

https://huagongshe.com/ko/reaction/4514

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-Amino-2-chlorophenolHCID 77578—
반응물2,5-DichloropyrimidineHCID 590641—
반응물N-(2-nitrobenzoyl)-N'-[3-chloro-4-(5-chloro-2-pyrimidinyloxy)phenyl]ureaHCID 13771441—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물3-Chloro-4-[(5-chloropyrimidin-2-yl)oxy]anilineHCID 14097091—

반응 단계

N-(2-nitrobenzoyl)-N'-[3-chloro-4-(5-chloro-2-pyrimidinyloxy)phenyl]urea (1) Into a flask, 1.50 g of 2,5-dichloropyrimidine, 1.45 g of 4-amino-2-chlorophenol, 2.76 g of potassium carbonate and 15 ml of dimethylsulfoxide, were introduced, and reacted in a nitrogen atmosphere at 100° C. for 1.5 hours under stirring. After the completion of the reaction, the product was poured into water, and extracted with diethyl ether. The extract was washed with a saturated sodium chloride aqueous solution, and dried over anhydrous sodium sulfate, and then the solvent was distilled off. The crude product thereby obtained was purified and isolated by silica gel column chromatography to obtain 2.20 g of 3-chloro-4-(5-chloro-2-pyrimidinyloxy)aniline having a melting point of from 95 to 96° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727077
출처 데이터셋uspto-grants-1988_02
ORD IDord-9d1b517cc1984e3fb05e9d6f78f2916e
출처 메모uspto-grants-1988_02