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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19627생성일: 2026년 10월 24일

2,3-Dichloropyridine → 6-(3-Chloropyridin-2-yl)-N-(4-fluorophenyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amine

https://huagongshe.com/ko/reaction/19627

반응식

참여 물질

역할이름HCID투입량
반응물2,3-DichloropyridineHCID 16988—
반응물DiisopropylethylamineHCID 81531—
반응물N-(4-fluorophenyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amineHCID 59346533—
용매dioxane N,N-dimethylacetamideHCID 67000103—
생성물6-(3-Chloropyridin-2-yl)-N-(4-fluorophenyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amineHCID 5934648930%

반응 조건

온도150 °C

반응 단계

N-(4-Fluorophenyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amine (0.47 g, 1.92 mmol) was dissolved in a mixture of dioxane/N,N-dimethylacetamide (4:1) (3 mL). To the mixture was added 2,3-dichloropyridine (420 mg, 2.86 mmol) and N,N-diisopropylethylamine (0.38 mL, 2.2 mmol). The mixture was heated at 150° C. in a Personal Chemistry microwave for 16 h. The solvents were removed under vacuum and the residue was dissolved in ethyl acetate and washed with sat. NaHCO3 and brine. The organic layer was dried over Na2SO4, filtered and evaporated to give a brown residue. The residue was purified by silica gel chromatography using a gradient of ethyl acetate:hexane (0-100%) to give the desired compound as an off-white powder (200 mg, 30%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745451B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-60bf7b0411ce46dcb33b6cf568ecec10
출처 메모uspto-grants-2010_06