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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19624생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/19624

반응식

참여 물질

역할이름HCID투입량
반응물2,3-DichloropyridineHCID 16988—
반응물DiisopropylethylamineHCID 81531—
반응물5,6,7,8-Tetrahydro-N-phenylpyrido[4,3-d]pyrimidin-4-amineHCID 59346558—
용매dioxane N,N-dimethylacetamideHCID 67000103—
생성물6-(3-Chloropyridin-2-yl)-5,6,7,8-tetrahydro-N-phenylpyrido[4,3-d]pyrimidin-4-amineHCID 5934647325.6%

반응 조건

온도150 °C

반응 단계

5,6,7,8-Tetrahydro-N-phenylpyrido[4,3-d]pyrimidin-4-amine (500 mg, 2.2 mmol) was dissoled in a mixture of dioxane/N,N-dimethylacetamide (4:1) (2 mL). To the mixture was added 2,3-dichloropyridine (423 mg, 2.86 mmol) and N,N-diisopropylethylamine (0.38 mL, 2.2 mmol). The mixture was heated at 150° C. in a microwave (Emrys Optimizer model, Personal Chemistry) 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 using a gradient of ethyl acetate:hexane (0-100%) to give the desired compound as an off-white powder (190 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745451B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-0254c620f8884a0a8f85c0b6c4abe0e9
출처 메모uspto-grants-2010_06