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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N,N-dimethyl-m-phenylenediamine | HCID 76084 | — |
| 반응물 | 6-((2-chloropyrimidin-4-yl)(methyl)amino)-N,2-dimethylbenzofuran-3-carboxamide | HCID 59224747 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 6-((2-(3-(dimethylamino)phenylamino)pyrimidin-4-yl)(methyl)amino)-N,2-dimethylbenzofuran-3-carboxamide | HCID 44634483 | 78% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07737157B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-6319f4d90ee340cbb34c2715c3d9de01 |
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| 출처 메모 | uspto-grants-2010_06 |
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