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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-Iodosuccinimide | HCID 120273 | — |
| 반응물 | 2-(1-bromopropyl)-6-methyl-4H-pyrido[1,2-a]pyrimidin-4-one | HCID 66864208 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 2-(1-bromopropyl)-3-iodo-6-methyl-4H-pyrido[1,2-a]pyrimidin-4-one | HCID 66864144 | 90.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09434746B2 |
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| 출처 데이터셋 | uspto-grants-2016_09 |
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| ORD ID | ord-a1a37df2a7c047c4a48b07db83119876 |
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| 출처 메모 | uspto-grants-2016_09 |
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