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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1810956생성일: 2026년 10월 27일

Ammonium Chloride → 2-{4-[2-(3,5-Dimethyl-pyrazol-1-yl)-acetyl]-piperazin-1-yl}-benzoic acid methyl ester

https://huagongshe.com/reaction/1810956

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물(3,5-Dimethyl-1H-pyrazol-1-yl)acetic acidHCID 572875—
반응물Bis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
반응물Methyl 2-(piperazin-1-yl)benzoateHCID 10932975—
용매Ethyl AcetateHCID 8857—
생성물2-{4-[2-(3,5-Dimethyl-pyrazol-1-yl)-acetyl]-piperazin-1-yl}-benzoic acid methyl esterHCID 6659972986%

반응 단계

To a vial containing the 2-piperazin-1-yl-benzoic acid methyl ester (0.667 g, 3.03 mmol) is added a pre-mixed solution containing (3,5-dimethyl-pyrazol-1-yl)-acetic acid (0.428 g, 2.78 mmol) and carbonyl dimidazole (0.567 g, 3.50 mmol). The mixture is stirred overnight and then diluted with 200 mL of EtOAc followed by 200 mL of saturated NH4Cl. The organic phase is washed with 2×200 mL of H2O and 1×200 mL of brine, dried (MgSO4), filtered and concentrated to give 0.849 g of 2-{4-[2-(3,5-dimethyl-pyrazol-1-yl)-acetyl]-piperazin-1-yl}-benzoic acid methyl ester in 86% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08362249B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-5dc9f5d4f3534a918efb13f11835813a
출처 메모uspto-grants-2013_01