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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 368753생성일: 2026년 10월 26일

4-(Trifluoromethyl)benzenesulfonyl chloride → Methyl 4-(2-chloro-5-methoxy-phenoxy)-3-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-5-(4-trifluoromethyl-benzenesulphonylamino)-benzoate

https://huagongshe.com/reaction/368753

반응식

참여 물질

역할이름HCID투입량
반응물4-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2777399—
반응물Methyl 3-amino-4-(2-chloro-5-methoxy-phenoxy)-5-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-benzoateHCID 23288632—
생성물Methyl 4-(2-chloro-5-methoxy-phenoxy)-3-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-5-(4-trifluoromethyl-benzenesulphonylamino)-benzoateHCID 23288596—

반응 단계

Analogously to Example 77, by condensing methyl 3-amino-4-(2-chloro-5-methoxy-phenoxy)-5-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-benzoate with 4-(trifluoromethyl)-benzenesulphonyl chloride there was obtained methyl 4-(2-chloro-5-methoxy-phenoxy)-3-[2-(tetrahydro-pyran-2-yloxy)-ethoxy]-5-(4-trifluoromethyl-benzenesulphonylamino)-benzoate and therefrom by treatment with 5.5M HCl there was obtained methyl 4-(2-chloro-5-methoxy-phenoxy)-3-(2-hydroxy-ethoxy)-5-(4-trifluoromethyl-benzenesulphonylamino)-benzoate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06133442
출처 데이터셋uspto-grants-2000_10
ORD IDord-54c0b4103e5a4d3dbfbc19b6aefd26c1
출처 메모uspto-grants-2000_10