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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16238생성일: 2026년 10월 25일

N,N-dimethyl-m-phenylenediamine → 6-((2-(3-(dimethylamino)phenylamino)pyrimidin-4-yl)(methyl)amino)-N,2-dimethylbenzofuran-3-carboxamide

https://huagongshe.com/reaction/16238

반응식

참여 물질

역할이름HCID투입량
반응물N,N-dimethyl-m-phenylenediamineHCID 76084—
반응물6-((2-chloropyrimidin-4-yl)(methyl)amino)-N,2-dimethylbenzofuran-3-carboxamideHCID 59224747—
용매DimethylformamideHCID 6228—
생성물6-((2-(3-(dimethylamino)phenylamino)pyrimidin-4-yl)(methyl)amino)-N,2-dimethylbenzofuran-3-carboxamideHCID 4463448378%

반응 조건

온도60 °C

반응 단계

6-((2-chloropyrimidin-4-yl)(methyl)amino)-N,2-dimethylbenzofuran-3-carboxamide (0.1 mmol) and 3-dimethylaminoaniline (0.1 mmol) were dissolved in 0.5 ml DMF. To this was added p-TsOH monohydrate (0.2 mmol). The reaction mixture was stirred at 60° C. for 5 hours, and subjected to extraction with EtOAc. Then water was added and the mixture was subjected to extraction with ethyl acetate. The organic layer was washed with water and brine sequentially, dried over anhydrous Na2SO4, and concentrated. The resulting residue was purified by column chromatography to provide the title product in a yield of 78%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737157B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-6319f4d90ee340cbb34c2715c3d9de01
출처 메모uspto-grants-2010_06