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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18936생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/18936

반응식

참여 물질

역할이름HCID투입량
반응물DiethylamineHCID 8021—
반응물Phosphorus pentachlorideHCID 24819—
반응물2-Piperazinone, 3,3-dimethyl-HCID 211157—
반응물Sodium BicarbonateHCID 516892—
반응물5-tert-butyl-2-nitro-1H-pyrrole-3-carboxylic acidHCID 58679298—
용매BenzeneHCID 241—
용매DichloromethaneHCID 6344—
생성물4-(2-tert-butyl-5-nitro-1H-pyrrole-4-carbonyl)-3,3-dimethylpiperazin-2-oneHCID 5867936749%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741479B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-f5ad1f4198a44773b190983f0e144bdc
출처 메모uspto-grants-2010_06