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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 573250생성일: 2026년 10월 26일

1,2,3,4-Tetrahydro-1-naphthalenol → 1,2,3,4-Tetrahydronaphthalen-1-yl 2-(1-{[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/573250

반응식

참여 물질

역할이름HCID투입량
반응물1,2,3,4-Tetrahydro-1-naphthalenolHCID 10723—
반응물TriphenylphosphineHCID 11776—
반응물2-[1-[[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl]-4-piperidinyl]-4-thiazolecarboxylic acidHCID 66601457—
용매TetrahydrofuranHCID 8028—
생성물1,2,3,4-Tetrahydronaphthalen-1-yl 2-(1-{[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazole-4-carboxylateHCID 44462769—

반응 단계

At room temperature, 1,2,3,4-tetrahydronaphthalen-1-ol (155 mg) and triphenylphosphine (758 mg) are added to a solution of 2-(1-{[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazole-4-carboxylic acid (III-4, 380 mg) in tetrahydrofuran (2.5 ml). The mixture is stirred at 0 C under argon for 5 minutes, and diethyldiazene 1,2-dicarboxylate (383 mg) is then added dropwise. The reaction mixture is slowly warmed to room temperature. After 2 hours, the solvent is removed under reduced pressure and the residue is purified chromatographically. This gives 1,2,3,4-tetrahydronaphthalen-1-yl 2-(1-{[5-methyl-3-(trifluoromethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazole-4-carboxylate (196 mg, 39%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09029549B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-f11035b402324518b92dffa295e6e131
출처 메모uspto-grants-2015_05