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HRID 73315生成日期:2026年10月23日

氨 → 1-[4-((1S,2S)-2-{[(2R)-2-methylpyrrolidin-1-yl]methyl}cyclopropyl)phenyl]pyrrolidin-2-one

https://huagongshe.com/zh-CN/reaction/73315

反应方程式

参与物

角色名称HCID投料
反应物氨HCID 222—
反应物3-哒嗪酮HCID 68153—
反应物(R)-1-(((1S,2S)-2-(4-bromophenyl)cyclopropyl)methyl)-2-methylpyrrolidineHCID 66796087—
产物1-[4-((1S,2S)-2-{[(2R)-2-methylpyrrolidin-1-yl]methyl}cyclopropyl)phenyl]pyrrolidin-2-oneHCID 44199260—

反应步骤

The title compound was prepared using the procedure described in Example 35B substituting pyrrolidin-2-one for pyridazin-3(2H)-one and substituting the product from Example 35A for the product from Example 34F. 1H NMR (300 MHz, CD3OD) δ 0.89-0.96 (m, 1H), 1.01-0.08 (m, 1H), 1.22 (d, J=6 Hz, 3H), 1.25-1.30 (m, 1H), 1.48-1.55 (m, 1H), 1.8-1.89 (m, 4H), 2.03-2.27 (m, 4H), 2.57 (t, J=6 Hz, 2H), 2.65-2.74 (m, 1H), 3.22 (q, J=6 Hz, 1H), 3.33-3.40 (m, 1H), 3.89 (t, J=6 Hz, 2H), 7.10 (d, J=9 Hz, 2H), 7.46 (d, J=9 Hz, 2H). MS (DCl—NH3) m/z 299 (M+H)+.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US08829041B2
来源数据集uspto-grants-2014_09
ORD IDord-ff3ae7bcbe6e475d929323ba5b739d05
来源说明uspto-grants-2014_09