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HRID 19624作成日:2026年10月25日

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

https://huagongshe.com/reaction/19624

反応式

関与物質

役割名称HCID仕込み量
反応物2,3-DichloropyridineHCID 16988—
反応物DiisopropylethylamineHCID 81531—
反応物5,6,7,8-Tetrahydro-N-phenylpyrido[4,3-d]pyrimidin-4-amineHCID 59346558—
溶媒dioxane N,N-dimethylacetamideHCID 67000103—
生成物6-(3-Chloropyridin-2-yl)-5,6,7,8-tetrahydro-N-phenylpyrido[4,3-d]pyrimidin-4-amineHCID 5934647325.6%

反応条件

温度150 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745451B2
出典データセットuspto-grants-2010_06
ORD IDord-0254c620f8884a0a8f85c0b6c4abe0e9
出典メモuspto-grants-2010_06