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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1472550생성일: 2026년 10월 25일

Cesium carbonate → 2-({5-Chloro-2-[(1,3-dimethyl-1H-pyrazol-4-yl)-amino]-4-pyridinyl}amino)-N-(methyloxy)benzamide

https://huagongshe.com/reaction/1472550

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물Binap, (A+-)-HCID 634876—
반응물1,3-dimethyl-1H-pyrazol-4-amineHCID 4431056—
반응물2-[(2,5-dichloro-4-pyridinyl)amino]-N-(methyloxy)benzamideHCID 57516896—
촉매palladium(II) acetateHCID 167845—
용매Dioxane tetrahydrofuranHCID 22018518—
생성물2-({5-Chloro-2-[(1,3-dimethyl-1H-pyrazol-4-yl)-amino]-4-pyridinyl}amino)-N-(methyloxy)benzamideHCID 4460951118%

반응 조건

온도140 °C

반응 단계

A microwave tube was charged with 2-[(2,5-dichloro-4-pyridinyl)amino]-N-(methyloxy)benzamide (250 mg, 0.8 mmol), 1,3-dimethyl-1H-pyrazol-4-amine (187 mg, 1.68 mmol), cesium carbonate (783 mg, 2.4 mmol) and dioxane/THF (3:1 ml). The reaction mixture was degassed under nitrogen for 10 min and palladium (II) acetate (9 mg, 0.04 mmol) and BINAP (50 mg, 0.08 mmol) were added. The mixture was stirred in a microwave at 140° C. for 40 min. It was evaporated and the residue dissolved in MeOH was filtered thru celite and thru an Acrodisc and purified further using preparative Agilent HPLC (5 to 95% water:acetonitrile with 0.1% formic acid). Fractions were combined and evaporated. Ether was added to the residue and a tan precipitate crashed out. It was filtered off and dried under vacuum at 40° C. for 2 days to afford the desired product (55 mg, 18%) as a tan solid. LC-MS (ES) m/z=387.1, [M+H]+=389.1. 1H NMR (400 MHz, DMSO-d6) ppm 11.93 (br. s., 1 H) 9.51 (br. s., 1 H) 8.03 (s, 1 H) 7.96 (s, 1 H) 7.82 (s, 1 H) 7.51-7.61 (m, 3 H) 7.07-7.15 (m, 1 H) 6.68 (s, 1 H) 3.70 (d, J=4.29 Hz, 6 H) 2.07 (s, 3 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09012479B2
출처 데이터셋uspto-grants-2015_04
ORD IDord-c92f6648e25a4b29b2a26961092e595e
출처 메모uspto-grants-2015_04