戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1723031作成日:2026年10月25日

Potassium Carbonate → 4-(4-Hydroxyphenyl)-1-(3,4-dihydro-3-methyl-2-phenylpyrimidin-4-on-6-ylmethyl)piperazine

https://huagongshe.com/reaction/1723031

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物p-(1-Piperazinyl)phenolHCID 92467—
反応物6-Chloromethyl-3,4dihydro-3-methyl-2-phenylpyrimidin-4-oneHCID 20026480—
生成物4-(4-Hydroxyphenyl)-1-(3,4-dihydro-3-methyl-2-phenylpyrimidin-4-on-6-ylmethyl)piperazineHCID 1407427065.6%

反応手順

According to the same procedure as described in Example 20, starting from 3.39 g (19 mmol) of 1-(4-hydroxyphenyl)piperazine and 4.20 g (17.9 mmol) of 6-chloromethyl-3,4dihydro-3-methyl-2-phenylpyrimidin-4-one, using 1.24 g (9 mmol) of K2CO3, 4.42 g (=65.6% yield) of 4-(4-hydroxyphenyl)-1-(3,4-dihydro-3-methyl-2-phenylpyrimidin-4-on-6-ylmethyl)piperazine were obtained; melting point 206°-207° C., analysis: C22H24N4O2 (MW 376.46) calc. C 70.19 H6.43 , N 14.88; found C 69.2, H 6.4, N 14.5%. For workup of the reaction mixture, the DMF had been evaporated off in vacuo, the residue had been taken up in water/CH2Cl2 and neutralized, and the CH2Cl2 extract residue had been crystallized from CH3OH.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04859670
出典データセットuspto-grants-1989_08
ORD IDord-3c61cb17e4514386bfdf5b93fbbdd036
出典メモuspto-grants-1989_08