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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1418329생성일: 2026년 10월 27일

Hydrochloric Acid → 4-t-butyl-N-[2,6-dichloro-5-(2-methoxyphenoxy)-4-pyrimidinyl]benzenesulfonamide

https://huagongshe.com/reaction/1418329

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물WaterHCID 962—
반응물5-(2-Methoxyphenoxy)-2,4,6-trichloropyrimidineHCID 53746905—
반응물p-t-Butylbenzenesulfonamide potassiumHCID 66748434—
용매Dimethyl SulfoxideHCID 679—
생성물4-t-butyl-N-[2,6-dichloro-5-(2-methoxyphenoxy)-4-pyrimidinyl]benzenesulfonamideHCID 8675387265.1%

반응 단계

5-(2-Methoxyphenoxy)-2,4,6-trichloropyrimidine (4) (4.8 g; 15.6 mmol) was dissolved in dimethyl sulfoxide (45 ml). Potassium 4-t-butylbenzenesulfonamide (8.0 g; 32 mmol) was added to the mixture while being cooled on ice, and the mixture was stirred for 30 minutes at room temperature. The reaction mixture was poured into water, made acidic with hydrochloric acid, and extracted with ethyl acetate, washed with water, dried over anhydrous sodium sulfate, and evaporated. The residue was recrystallized from ether, to thereby obtain 4.9 g (yield: 65%) of the title compound as colorless needles.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05883092
출처 데이터셋uspto-grants-1999_03
ORD IDord-acd06b1c272d490387309d944c801387
출처 메모uspto-grants-1999_03