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HRID 18936作成日:2026年10月25日

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

https://huagongshe.com/reaction/18936

反応式

関与物質

役割名称HCID仕込み量
反応物DiethylamineHCID 8021—
反応物Phosphorus pentachlorideHCID 24819—
反応物2-Piperazinone, 3,3-dimethyl-HCID 211157—
反応物Sodium BicarbonateHCID 516892—
反応物5-tert-butyl-2-nitro-1H-pyrrole-3-carboxylic acidHCID 58679298—
溶媒BenzeneHCID 241—
溶媒DichloromethaneHCID 6344—
生成物4-(2-tert-butyl-5-nitro-1H-pyrrole-4-carbonyl)-3,3-dimethylpiperazin-2-oneHCID 5867936749%

反応手順

To 5-tert-butyl-2-nitro-1H-pyrrole-3-carboxylic acid (100 mg, 0.47 mmol) in benzene (2 mL) was added solid PCl5 (120 mg, 0.57 mmol). The resulting reaction mixture was stirred at RT until all the PCl5 went into the solution. This reaction mixture was then added to 3,3-dimethylpiperazin-2-one (120 mg, 0.94 mmol) and diethylamine (280 ml, 0.94 mmol) in dichloromethane (DCM) (3 mL). After 30 min, the reaction was diluted with DCM (10 mL) and followed by addition of sat. NaHCO3. The organic phase was then washed with 1N HCl and brine, dried, and concentrated in vacuo. This crude product was further purified using flash chromatography (EtOAc/Hexane: 1/4) to provide 4-(2-tert-butyl-5-nitro-1H-pyrrole-4-carbonyl)-3,3-dimethylpiperazin-2-one 6 (74 mg, 49%) as yellow foam.

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-f5ad1f4198a44773b190983f0e144bdc
出典メモuspto-grants-2010_06