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HRID 970310作成日:2026年10月24日

Piperazine → Cgp-74588

https://huagongshe.com/ja/reaction/970310

反応式

関与物質

役割名称HCID仕込み量
反応物PiperazineHCID 4837—
反応物4-(Chloromethyl)-N-(4-methyl-3-((4-(3-pyridinyl)-2-pyrimidinyl)amino)phenyl)benzamideHCID 10181075—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物Cgp-74588HCID 9869737—

反応手順

25.8 g (300 mmol) of piperazine are suspended in a mixture of 25 ml of ethanol and 25 ml of water. After almost a clear solution has formed, 12.9 g (30 mmol) of 4-chloromethyl-N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-phenyl]-benzamide are added step by step. The yellow solution is boiled under reflux for 14 hours, cooled to room temperature and filtered over Celite. 100 ml of water is added to the solution, the ethanol is evaporated under vacuum and 30 ml of 1N NaOH is added, leading to crystallization of the product. Drying at 50 mbar and 60° C. yields N-[4-methyl-3-(4-pyridin-3-yl-pyrimidin-2-ylamino)-phenyl]-4-piperazin-1-ylmethyl-benzamide; Rf=0.15 (methylene chloride:ethyl acetate:methanol:conc. aqueous ammonium hydroxide solution=60:10:30:2); tR (HPLC)2) 14.6 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07312216B2
出典データセットuspto-grants-2007_12
ORD IDord-bda9621ad94543d4bb433a1bdaebf06b
出典メモuspto-grants-2007_12