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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 982668생성일: 2026년 10월 26일

Triethylamine → 4-[3-[5-[4-(4-Cyanobenzoyl)piperazin-1-yl]pentyl]-2,5-dihydro-4-methyl-2,5-dioxo-1H-pyrrol-1-yl]-2-(trifluoromethyl)benzonitrile

https://huagongshe.com/reaction/982668

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-Cyanobenzoyl chlorideHCID 80172—
반응물4-[2,5-dihydro-3-methyl-2,5-dioxo-4-[5-(piperazin-1-yl)pentyl]-1H-pyrrol-1-yl]-2-(trifluoromethyl)benzonitrileHCID 22562427—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물4-[3-[5-[4-(4-Cyanobenzoyl)piperazin-1-yl]pentyl]-2,5-dihydro-4-methyl-2,5-dioxo-1H-pyrrol-1-yl]-2-(trifluoromethyl)benzonitrileHCID 10175095—

반응 단계

0.2 ml of a solution of triethylamine in tetrahydrofuran (1.5 mol/l) and 7 mg of 4-cyanobenzoyl chloride in 0.4 ml of tetrahydrofuran were added to a solution of 9 mg of 4-[2,5-dihydro-3-methyl-2,5-dioxo-4-[5-(piperazin-1-yl)-pentyl]-1H-pyrrol-1-yl]-2-(trifluoromethyl)benzonitrile in 0.4 ml of tetrahydrofuran, and the mixture was stirred for 8 hours at room temperature. For working-up, the reaction mixture was diluted with ethyl acetate and washed with semi-saturated sodium bicarbonate solution. After the organic phase was concentrated by evaporation, it was chromatographed with methanol/dichloromethane on silica gel, and 7 mg of the title compound was thus obtained as a yellowish oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06861432B2
출처 데이터셋uspto-grants-2005_03
ORD IDord-dba61ea9c7b1451d910e35d739749500
출처 메모uspto-grants-2005_03