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HRID 130415作成日:2026年10月25日

Triethylamine → 4-(cis-3,5-Dimethyl-1-piperazinyl)-2-nitrobenzonitrile

https://huagongshe.com/reaction/130415

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-Chloro-2-nitrobenzonitrileHCID 96924—
反応物rel-(2R,6S)-2,6-dimethylpiperazineHCID 6950261—
反応物Sodium MethoxideHCID 10942334—
触媒2-(2'-Di-tert-butylphosphine)biphenylpalladium(II) acetateHCID 11982262—
生成物4-(cis-3,5-Dimethyl-1-piperazinyl)-2-nitrobenzonitrileHCID 69198156—

反応条件

温度85 °C

反応手順

A mixture of 4-chloro-2-nitrobenzonitrile (Tetrahedron 1994, 50, 5515-5126) (650 mg, 3.56 mmol), sodium methoxide (270 mg, 5.00 mmol) and acetato-(2′-di-tert-butylphosphino-1,1′-biphenyl-2-yl)palladium (II) (115 mg, 0.25 mmol) was treated with triethylamine (0.25 ml, 1.79 mmol) followed by cis-2,6-dimethylpiperazine (488 mg, 4.27 mmol) and the mixture heated to 85° C. under an inert atmosphere over 30 minutes. The mixture was then kept at this temperature for 16 hours. The mixture was then filtered through kieselguhr, washing with toluene (50 ml) and the filtrate reduced in vacuo. The residue was then purified using an SCX ion exchange cartridge (Varian bond-elute) eluting with methanol followed by 2M ammonia in methanol to afford a dark residue which was purified by mass directed autoprep BPLC to afford the title compound as the formic acid salt. MS (ES+) m/e 261 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07381728B2
出典データセットuspto-grants-2008_06
ORD IDord-c9f26323c77a4bdebefe7106d812054a
出典メモuspto-grants-2008_06