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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17952생성일: 2026년 10월 24일

Potassium Carbonate → 1-Benzo[1,3]dioxol-5-yl-cyclopropanecarboxylic Acid[5-(2,4-dimethoxy-phenyl)-pyridin-2-yl]-amide

https://huagongshe.com/ko/reaction/17952

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2,4-Dimethoxybenzeneboronic acidHCID 2734341—
반응물1-(benzo[d][1,3]dioxol-5-yl)-N-(5-bromopyridin-2-yl)cyclopropanecarboxamideHCID 59166163—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매DimethylformamideHCID 6228—
생성물1-Benzo[1,3]dioxol-5-yl-cyclopropanecarboxylic Acid[5-(2,4-dimethoxy-phenyl)-pyridin-2-yl]-amideHCID 16679709—

반응 조건

온도80 °C

반응 단계

1-Benzo[1,3]dioxol-5-yl-cyclopropanecarboxylic acid (5-bromo-pyridin-2-yl)-amide (36.1 mg, 0.10 mmol) was dissolved in 1 mL of N,N-dimethylformamide in a reaction tube. 2,4-Dimethoxybenzeneboronic acid (24 mg, 0.13 mmol), 0.1 mL of an aqueous 2 M potassium carbonate solution, and a catalytic amount of Pd(dppf)Cl2 (6.6 mg, 0.0090 mmol) were added and the reaction mixture was heated at 80° C. for three hours. The resulting material was cooled to room temperature, filtered, and purified by reverse-phase preparative liquid chromatography to yield the pure product as a trifluoroacetic acid salt. ESI-MS m/z calc. 418.2. found 419.0 (M+1)+. Retention time 3.18 minutes. 1H NMR (400 MHz, CD3CN) δ 1.25-1.29 (m, 2H), 1.63-1.67 (m, 2H), 3.83 (s, 3H), 3.86 (s, 3H), 6.04 (s, 2H), 6.64-6.68 (m, 2H), 6.92 (d, J=8.4 Hz, 1H), 7.03-7.06 (m, 2H), 7.30 (d, J=8.3 Hz, 1H), 7.96 (d, J=8.9 Hz, 1H), 8.14 (dd, J=8.9, 2.3 Hz, 1H), 8.38 (d, J=2.2 Hz, 1H), 8.65 (s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741321B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-774623a2cf324b43a74d60b03b0f1b8f
출처 메모uspto-grants-2010_06