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HRID 2294042作成日:2026年10月25日

1-(2-Methoxyphenyl)piperazine → 5-[4-(2-Methoxy-phenyl)-piperazin-1-ylmethyl]-pyrimidine-2,4-diamine

https://huagongshe.com/reaction/2294042

反応式

関与物質

役割名称HCID仕込み量
反応物1-(2-Methoxyphenyl)piperazineHCID 1346—
反応物TriethylamineHCID 8471—
反応物5-(Bromomethyl)pyrimidine-2,4-diamine dihydrobromideHCID 21473608—
溶媒TetrahydrofuranHCID 8028—
生成物5-[4-(2-Methoxy-phenyl)-piperazin-1-ylmethyl]-pyrimidine-2,4-diamineHCID 2147362338%

反応手順

A solution of 3.2 g (0.017 mol) of 1-(2-methoxy-phenyl)-piperazine in 100 ml of tetrahydrofuran was treated with 11.6 ml (0.084 mol) of triethylamine and 6.1 g (0.017 mol) of 5-bromomethyl-pyrimidine-2,4-diamine dihydrobromide and the mixture was stirred at room temperature under argon for 16 hours. The suspension obtained was suction filtered and the filtrate was completely freed from the solvents. The residue was chromatographed over silica gel with acetonitrile/methanol 1:1 as the eluent and digested in diethyl ether. 2.0 g (38%) of 5-[4-(2-methoxy-phenyl)-piperazin-1-ylmethyl]-pyrimidine-2,4-diamine were obtained as white crystals; m.p. 195°-196°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05688798
出典データセットuspto-grants-1997_11
ORD IDord-404fb7722fae4ab8bb4f3f2f95206a85
出典メモuspto-grants-1997_11