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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 486640생성일: 2026년 10월 25일

4-tert-Butylbenzenesulfonamide → p-tert-butyl-N-[6-(2-hydroxyethoxy)-5(o-methoxyphenoxy)-2-(trifluoromethyl)-4-pyrimidinyl]benzenesulfonamide

https://huagongshe.com/reaction/486640

반응식

참여 물질

역할이름HCID투입량
반응물4-tert-ButylbenzenesulfonamideHCID 222872—
반응물4,6-Dichloro-5-(2-methoxyphenoxy)-2-trifluoromethylpyrimidineHCID 18184264—
용매TolueneHCID 1140—
생성물p-tert-butyl-N-[6-(2-hydroxyethoxy)-5(o-methoxyphenoxy)-2-(trifluoromethyl)-4-pyrimidinyl]benzenesulfonamideHCID 19095722—

반응 단계

By reacting 4,6-dichloro-5-(2-methoxyphenoxy)-2-trifluoromethylpyrimidine with p-tert-butylbenzenesulfonamide and with ethylene glycol Na there was obtained p-tert-butyl-N-[6-(2-hydroxyethoxy)-5(o-methoxyphenoxy)-2-(trifluoromethyl)-4-pyrimidinyl]benzenesulfonamide, m.p. 190°-192° C. (from toluene). Sodium salt: M.p. 288°-289° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05292740
출처 데이터셋uspto-grants-1994_03
ORD IDord-fdd360d13d074b359c24049046676f2f
출처 메모uspto-grants-1994_03