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HRID 421356生成日期:2026年10月23日

反式-2,5-二甲基哌嗪 → 5-[8-(trans-2,5-Dimethylpiperazin-1-yl)-9-isobutyl-6-morpholin-4-yl-9H-purin-2-yl]pyrimidin-2-amine

https://huagongshe.com/zh-CN/reaction/421356

反应方程式

参与物

角色名称HCID投料
反应物反式-2,5-二甲基哌嗪HCID 220672—
反应物5-(8-Chloro-9-isobutyl-6-morpholino-9H-purin-2-yl)pyrimidin-2-amineHCID 59333549—
溶剂N-甲基吡咯烷酮HCID 13387—
产物5-[8-(trans-2,5-Dimethylpiperazin-1-yl)-9-isobutyl-6-morpholin-4-yl-9H-purin-2-yl]pyrimidin-2-amineHCID 6665871298.9%

反应条件

温度150 °C

反应步骤

trans-2,5-Dimethylpiperazine (150 mg, 1.3 mmol) and N-methylpyrrolidone (1 ml) were added to 5-(8-chloro-9-isobutyl-6-morpholin-4-yl-9H-purin-2-yl)pyrimidin-2-amine (100 mg, 0.26 mmol) and the resulting mixture was stirred at 150° C. for 48 hours. The reaction mixture was cooled and partitioned with methylene chloride and water, the organic layer was dried over magnesium sulfate, and the solvent was concentrated under reduced pressure. The residue was purified by preparative HPLC (column, NOMURA Develosil Combi-RP-5; mobile phase, acetonitrile/water/formic acid) to give the title compound (120 mg) as a pale yellow solid.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US08097622B2
来源数据集uspto-grants-2012_01
ORD IDord-65687781f1df46848595e6d42acdc07c
来源说明uspto-grants-2012_01