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HRID 1663201生成日期:2026年10月24日

2-氨基-4-甲基吡啶 → 2-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-N-(4-methyl-pyridin-2-yl)acetamide

https://huagongshe.com/zh-CN/reaction/1663201

反应方程式

参与物

角色名称HCID投料
反应物2-氨基-4-甲基吡啶HCID 1533—
反应物三乙胺HCID 8471—
反应物胸腺嘧啶-1-乙酸HCID 853753—
反应物Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
溶剂N,N-二甲基甲酰胺HCID 6228—
产物2-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-N-(4-methyl-pyridin-2-yl)acetamideHCID 24745170—

反应步骤

A mixture of 2-(5-methyl-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)acetic acid (75 mg, 0.4 mmol), 4-methylpyridin-2-amine (44 mg, 0.4 mmol), HBTU (151 mg, 0.4 mmol) and 0.1 mL of Et3N in DMF (5 mL) was stirred at room temperature for 2 hours to provide the title compound, which was then purified by HPLC. 1H NMR (400 MHz, DMSO-d6) δ: 11.37 (s, 1H), 10.97 (s, 1H), 8.20 (d, J=8.0 Hz, 1H), 7.81 (s, 1H), 7.51 (s, 1H), 7.03 (d, J=8.0 Hz, 1H), 4.58 (s, 2H), 2.33 (s, 3H), 1.77 (s, 3H). [M+H] calc'd for C13H14N4O2, 275; found, 275.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US08034822B2
来源数据集uspto-grants-2011_10
ORD IDord-45ccae9971ee40cc8e3ac3e0296fb6a9
来源说明uspto-grants-2011_10