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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18933생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Phosphorus pentachlorideHCID 24819—
반응물DiisopropylethylamineHCID 81531—
반응물2-Piperazinone, 3,3-dimethyl-HCID 211157—
반응물5-tert-butyl-3-nitro-1H-pyrrole-2-carboxylic acidHCID 18322391—
용매DichloromethaneHCID 6344—
생성물4-(2-tert-butyl-4-nitro-1H-pyrrole-5-carbonyl)-3,3-dimethylpiperazin-2-oneHCID 5867927253.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741479B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-322741f3750e433294754e2aba2b83fd
출처 메모uspto-grants-2010_06