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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1804013생성일: 2026년 10월 25일

1-Hydroxybenzotriazole → (4-Bromo-3-fluorophenyl)[4-(3,5-dimethylpyridin-2-yl)piperazin-1-yl]methanone

https://huagongshe.com/reaction/1804013

반응식

참여 물질

역할이름HCID투입량
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물4-Bromo-3-fluorobenzoic acidHCID 2773341—
반응물1-(3,5-Dimethylpyridin-2-yl)piperazineHCID 58484496—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물(4-Bromo-3-fluorophenyl)[4-(3,5-dimethylpyridin-2-yl)piperazin-1-yl]methanoneHCID 5848457267.4%

반응 단계

1-(3,5-Dimethylpyridin-2-yl)piperazine (2.87 g) described in Preparation Example 47 was dissolved in N,N-dimethylformamide (38 ml), 4-bromo-3-fluorobenzoic acid (3.29 g), 1-hydroxybenzotriazole 1 hydrate (2.43 g) and 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide hydrochloride (3.45 g) were added, and the mixture was stirred at room temperature for 4 hr. The reaction mixture was poured into water under cooling, and extracted with ethyl acetate. The organic layer was washed twice with water, washed with saturated brine, and dried over sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by column chromatography (ethyl acetate:hexane). Then, ethyl acetate and hexane were added and the mixture was stirred at room temperature. The solid was collected by filtration and dried under reduced pressure to give the title compound (3.97 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08354401B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-568f000455b64c37b998cac25f091c65
출처 메모uspto-grants-2013_01