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HRID 18933作成日:2026年10月24日

Phosphorus pentachloride → 4-(2-tert-butyl-4-nitro-1H-pyrrole-5-carbonyl)-3,3-dimethylpiperazin-2-one

https://huagongshe.com/ja/reaction/18933

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphorus pentachlorideHCID 24819—
反応物DiisopropylethylamineHCID 81531—
反応物2-Piperazinone, 3,3-dimethyl-HCID 211157—
反応物5-tert-butyl-3-nitro-1H-pyrrole-2-carboxylic acidHCID 18322391—
溶媒DichloromethaneHCID 6344—
生成物4-(2-tert-butyl-4-nitro-1H-pyrrole-5-carbonyl)-3,3-dimethylpiperazin-2-oneHCID 5867927253.1%

反応手順

The previously prepared 5-tert-butyl-3-nitro-1H-pyrrole-2-carboxylic acid (0.203 g, 1.11 mmol) and PCl5 (0.232 g, 1.11 mmol) were dissolved in dichloromethane (4 mL) and stirred at room temperature for 5 minutes. The resulting solution was added in one portion to a solution of 3,3-dimethylpiperazin-2-one (0.214 g, 1.67 mmol) and DIEA (0.288 g, 2.23 mmol) in dichloromethane (3 mL) and stirred at room temperature for 5 minutes. The reaction mixture was diluted with dichloromethane and washed sequentially with 1N aqueous HCl, saturated sodium bicarbonate, dried and the solvent removed under vacuum. The crude product was purified by chromatographic column (silica gel, dichloromethane:methanol, 95:5) to afford 0.190 g of expected 4-(2-tert-butyl-4-nitro-1H-pyrrole-5-carbonyl)-3,3-dimethylpiperazin-2-one.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741479B2
出典データセットuspto-grants-2010_06
ORD IDord-322741f3750e433294754e2aba2b83fd
出典メモuspto-grants-2010_06