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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 602134생성일: 2026년 10월 25일

Triethylamine → Methyl 3-[3-[[2-(4-Chlorophenyl)-4-methylthiazol-5-yl]carbonylaminomethyl]piperidin-1-yl]benzoate

https://huagongshe.com/reaction/602134

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물N-(Piperidin-3-yl methyl)-2-(4-chlorophenyl)-4-methylthiazole-5-carboxamideHCID 57572157—
반응물3-Methoxycarbonylphenylboric acidHCID 67170287—
촉매Cupric acetateHCID 8895—
용매DichloromethaneHCID 6344—
생성물Methyl 3-[3-[[2-(4-Chlorophenyl)-4-methylthiazol-5-yl]carbonylaminomethyl]piperidin-1-yl]benzoateHCID 6726711337%

반응 단계

N-(Piperidin-3-yl methyl)-2-(4-chlorophenyl)-4-methylthiazole-5-carboxamide (172 mg, 0.492 mmol), 3-(methoxycarbonyl)phenylboric acid (177 mg, 0.984 mmol) and molecular sieves 4 Å (400 mg) were suspended in dichloromethane (10 mL). To this suspension, copper (II) acetate (188 mg, 0.984 mmol) and triethylamine (0.344 mL, 2.46 mmol) were added and the mixture was stirred at room temperature for 8 hours. Subsequently, the reaction mixture was filtered through Celite, followed by addition of a saturated aqueous sodium bicarbonate solution. The mixture was then extracted with ethyl acetate and the extract washed with brine, followed by drying over magnesium sulfate and evaporation of the solvent. Purification of the residue by silica gel column chromatography (hexane:ethyl acetate=20:1->2:1) gave 88.2 mg (37%) of the desired compound as a colorless powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902367B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-242c2e22b9eb451bb9d6f24bbb2a730a
출처 메모uspto-grants-2011_03