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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1253771생성일: 2026년 10월 26일

Triphenylphosphine → 1-[3-(4-{4-[1-(2-Chloro-phenyl)-ethoxycarbonylamino]-3-methyl-isoxazol-5-yl}-phenyl)-prop-2-ynyl]-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1253771

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Diisopropyl diazene-1,2-dicarboxylateHCID 75555—
반응물Ethyl 3-(Trifluoromethyl)pyrazole-4-carboxylateHCID 596095—
반응물{5-[4-(3-Hydroxy-prop-1-ynyl)-phenyl]-3-methyl-isoxazol-4-yl}-carbamic acid 1-(2-chloro-phenyl)-ethyl esterHCID 70878238—
용매TetrahydrofuranHCID 8028—
생성물1-[3-(4-{4-[1-(2-Chloro-phenyl)-ethoxycarbonylamino]-3-methyl-isoxazol-5-yl}-phenyl)-prop-2-ynyl]-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid ethyl esterHCID 68529647—

반응 단계

To a solution of {5-[4-(3-hydroxy-prop-1-ynyl)-phenyl]-3-methyl-isoxazol-4-yl}-carbamic acid 1-(2-chloro-phenyl)-ethyl ester (0.200 g, 0.49 mmol), ethyl 5-(trifluoromethyl)-1H-pyrazole-4-carboxylate (0.101 g, 0.49 mmol), and triphenylphosphine (0.127 g, 0.49 mmol) in THF (4 mL) was added diisopropyl azodicarboxylate (0.10 mL, 0.49 mmol), and the reaction was stirred at room temperature for 2 hours. The mixture was concentrated, and the residue was purified by preparative HPLC to give the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08455499B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-3f35ad9b07114f939008e9fd17412984
출처 메모uspto-grants-2013_06