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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58224생성일: 2026년 10월 25일

N-Iodosuccinimide → 2-(1-bromopropyl)-3-iodo-6-methyl-4H-pyrido[1,2-a]pyrimidin-4-one

https://huagongshe.com/reaction/58224

반응식

참여 물질

역할이름HCID투입량
반응물N-IodosuccinimideHCID 120273—
반응물2-(1-bromopropyl)-6-methyl-4H-pyrido[1,2-a]pyrimidin-4-oneHCID 66864208—
용매AcetonitrileHCID 6342—
생성물2-(1-bromopropyl)-3-iodo-6-methyl-4H-pyrido[1,2-a]pyrimidin-4-oneHCID 6686414490.5%

반응 조건

온도80 °C

반응 단계

A mixture of 2-(1-bromopropyl)-6-methyl-4H-pyrido[1,2-a]pyrimidin-4-one (3.46 g, 12.3 mmol) and N-iodosuccinimide (4.15 g, 18.4 mmol) in acetonitrile (100 mL) was stirred at 80° C., under nitrogen, overnight. After removal of acetonitrile in vacuum, the resulting solid was dissolved in methylene chloride, washed with water, saturated Na2S2O3, saturated sodium bicarbonate, and brine; and then the organic layers dried over sodium sulfate and then filtered. The filtrate was concentrated under reduced pressure to provide the desired product (4.53 g, 90.4%). LCMS calculated for C12H13BrIN2O (M+H)+: m/z=406.9. Found: 407.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434746B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-a1a37df2a7c047c4a48b07db83119876
출처 메모uspto-grants-2016_09