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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 552167생성일: 2026년 10월 26일

Potassium Carbonate → 6-[4-Methyl-4-(2-trifluoromethylphenoxy)piperidin-1-YL]pyridazine-3-carboxylic acid (2-cyclopropylethyl)amide

https://huagongshe.com/reaction/552167

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물6-Chloro-N-(2-cyclopropylethyl)pyridazine-3-carboxamideHCID 65561565—
반응물4-Methyl-4-(2-trifluoromethylphenoxy)piperidineHCID 67171507—
촉매Tetrabutylammonium BromideHCID 74236—
용매1,4-DioxaneHCID 31275—
생성물6-[4-Methyl-4-(2-trifluoromethylphenoxy)piperidin-1-YL]pyridazine-3-carboxylic acid (2-cyclopropylethyl)amideHCID 1153963520%

반응 단계

To a stirred solution of 6-chloropyridazine-3-carboxylic acid (2-cyclopropylethyl)amide (0.020 g, 0.090 mmol) in dioxane (5 mL) was added 4-methyl-4-(2-trifluoromethylphenoxy)piperidine (0.015 g, 0.060 mmol), potassium carbonate (0.033 g, 0.240 mmol) and tetrabutyl ammonium bromide (0.002 g, 0.001 mmol). The resulting mixture was stirred at reflux for 48 hours, filtered and then concentrated in vacuo. The crude product was purified by column chromatography to yield the title compound in 20% yield (0.005 g). 1H NMR (300 MHz, CDCl3) δ 8.02-7.96 (m, 2H), 7.60-7.57 (m, 1H), 7.48-7.40 (m, 1H), 7.14-7.12 (d, J=8.0 Hz, 1H), 7.06-6.99 (m, 2H), 4.25-4.21 (m, 2H), 3.65-3.51 (m, 4H), 2.35-2.31 (m, 2H), 1.85-1.74 (m, 2H), 1.53-1.46 (dd, J=6.6 and 7.0 Hz, 2H), 1.20 (s, 3H), 0.77-0.69 (m, 1H), 0.48-0.42 (m, 2H), 0.11-0.05 (m, 2H). MS (ES+) m/z 449.4 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07951805B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-ecdf6e9ce59441179dbb6b993c0550da
출처 메모uspto-grants-2011_05