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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 704317생성일: 2026년 10월 26일

Triethylamine → N-[4-(5-chloro-2-pyrimidinyloxy)-3-methylphenyl]-2-nitrobenzenesulfenamide

https://huagongshe.com/reaction/704317

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Ethyl AcetateHCID 8857—
반응물2-Nitrobenzenesulfenyl chlorideHCID 24319—
반응물4-((5-Chloropyrimidin-2-yl)oxy)-3-methylanilineHCID 14207808—
용매TolueneHCID 1140—
생성물N-[4-(5-chloro-2-pyrimidinyloxy)-3-methylphenyl]-2-nitrobenzenesulfenamideHCID 1000036883.6%

반응 단계

2.0 g of 4-(5 chloro-2-pyrimidinyloxy)-3methylaniline and 0.94 g of triethylamine were dissolved in 20 ml of toluene, and a solution of 1.61 g of 2-nitrobenzenesulfenyl chloride dissolved in 5 ml of toluene was dropwise added thereto at room temperature. The mixture was reacted at room temperature for 1 hour under stirring. After completion of the reaction, ethyl acetate was added to the reaction product, and the ethyl acetate layer was washed with water, dried over Glauber's salt and then purified by column chromatography to obtain 2.76 g of N-[4-(5-chloro-2-pyrimidinyloxy)-3-methylphenyl]-2-nitrobenzenesulfenamide (Intermediate Compound No. 37) (melting point: 74°-85° C.) in a yellow non-crystalline form.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04987135
출처 데이터셋uspto-grants-1991_01
ORD IDord-635377d9a71e459093799c5dc60a7731
출처 메모uspto-grants-1991_01