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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80669생성일: 2026년 10월 25일

4-(3-Methanesulfonyloxymethyl-[1,2,4]triazol-1-yl)-piperidine-1-carboxylic acid tert-butyl ester → ethyl 1-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-3-(trifluoromethyl)-1H-pyrazole-4-carboxylate

https://huagongshe.com/reaction/80669

반응식

참여 물질

역할이름HCID투입량
반응물4-(3-Methanesulfonyloxymethyl-[1,2,4]triazol-1-yl)-piperidine-1-carboxylic acid tert-butyl esterHCID 57708378—
반응물1-(5-Ethylpyrimidin-2-yl)piperidin-4-yl methanesulfonateHCID 57708402—
반응물HCID 178469923HCID 178469923—
생성물ethyl 1-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-3-(trifluoromethyl)-1H-pyrazole-4-carboxylateHCID 57708415—
생성물ethyl 1-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylateHCID 57708422—

반응 단계

The compound was synthesized using ethyl 3-(trifluoromethyl)-1H-pyrazole-4-carboxylate and 1-(5-ethylpyrimidin-2-yl)piperidin-4-yl methanesulfonate in a manner similar to that described in Intermediate 1, Step 1. The reaction afforded two regioisomers, ethyl 1-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-3-(trifluoromethyl)-1H-pyrazole-4-carboxylate and ethyl 1-(1-(5-ethylpyrimidin-2-yl)piperidin-4-yl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxylate which were separated by flash column chromatography on silica gel.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846675B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-b8c9e44a77234097b3956546c756b42c
출처 메모uspto-grants-2014_09