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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 926537생성일: 2026년 10월 25일

Ammonia → 3-(4-(1H-Pyrazol-1-yl)benzyl)-6-bromo-2,4-dichloro-8-methylquinoline

https://huagongshe.com/reaction/926537

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참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물4-Bromo-2-methylanilineHCID 11423—
반응물Phosphorus oxychlorideHCID 24813—
반응물3-(4-(1H-pyrazol-1-yl)benzyl)-6-bromo-2,4-dichloroquinolineHCID 86715594—
용매WaterHCID 962—
생성물3-(4-(1H-Pyrazol-1-yl)benzyl)-6-bromo-2,4-dichloro-8-methylquinolineHCID 86715598—

반응 조건

온도105 °C

반응 단계

A mixture of 2-(4-(1H-pyrazol-1-yl)benzyl)malonic acid (20.0 g, 71.5 mmol, Intermediate 3: step b) and 4-bromo-2-methylaniline (13.3 g, 71.5 mmol) in phosphorus oxychloride (66.8 mL, 712 mmol) was heated at 105° C. After 5 hours, the mixture was cooled to 23° C. and added to water (600 mL) with cooling so that the internal temperature did not exceed 35° C. The pH of the mixture was adjusted to 8-9 by the slow addition of saturated aqueous ammonia solution such that the internal temperature did not exceed 35° C. After 30 minutes of stirring at room temperature, the mixture was filtered and the solid material was suspended in acetonitrile (200 mL), sonicated and filtered. The solid material was collected and suspended in DCM (80 mL), sonicated, filtered and washed with ether (40 mL). The filtrate was concentrated, suspended in DCM (40 mL), sonicated and filtered to provide more of the title compound. To 5 g of the isolated solid, DCM (300 mL) and saturated aqueous NaHCO3 (100 mL) were added and the mixture was transferred to a separatory funnel, and the layers were separated. The DCM layer was further washed with brine (100 mL), dried (MgSO4), filtered and the solvents were removed under reduced pressure. The crude material was purified using flash-column chromatography on silica gel eluting with DCM to provide the title compound as an off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09284308B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-8fca958a69c346d29a2848a976cdae07
출처 메모uspto-grants-2016_03