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HRID 1768947作成日:2026年10月27日

2-Naphthoxyacetic acid → 1-[2-(2-Naphthyloxy)acetyl]-4-[2,6-di(1-pyrrolidinyl)-4-pyrimidinyl]homopiperazine

https://huagongshe.com/reaction/1768947

反応式

関与物質

役割名称HCID仕込み量
反応物2-Naphthoxyacetic acidHCID 8422—
反応物1-[2,6-Di(1-pyrrolidinyl)-4-pyrimidinyl]homopiperazineHCID 18946301—
溶媒TetrahydrofuranHCID 8028—
生成物1-[2-(2-Naphthyloxy)acetyl]-4-[2,6-di(1-pyrrolidinyl)-4-pyrimidinyl]homopiperazineHCID 1894628628%

反応手順

To a solution of 2-(2-naphthyloxy)acetic acid (1.1 g, 5.0 mmol) in anhydrous tetrahydrofuran (25 ml) carbonyl-diimidazole (0.80 g, 5.0 mmol) was added in portions, under stirring at room temperature. After 15 minutes a solution of 1-[2,6-di(1-pyrrolidinyl)-4-pyrimidinyl]homopiperazine (1.58 g, 5.0 mmol) in anhydrous tetrahydrofuran (15 ml) was added dropwise. The mixture was stirred at room temperature for 8 hours and the solvent was distilled off under reduced pressure. The residue was dissolved in methylene chloride, the solution was washed three times with water, dried over MgSO4 and concentrated. The obtained crude product was chromatographed over a silica gel column eluting with a 1:2 mixture of benzene and ethyl acetate to afford 0.7 g of the title compound, yield: 28%, mp. 103°-110° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05380724
出典データセットuspto-grants-1995_01
ORD IDord-d6156057814448ad884c7ca6105d4e1e
出典メモuspto-grants-1995_01