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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 709972생성일: 2026년 10월 26일

Methyl iodide → 3-Methyl-2-(methylthio)-4(3H)-pyrimidinone

https://huagongshe.com/reaction/709972

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물2-(Methylthio)-1H-pyrimidin-4-oneHCID 79823—
반응물Lithium HexamethyldisilazideHCID 2733832—
용매DimethylformamideHCID 6228—
생성물3-Methyl-2-(methylthio)-4(3H)-pyrimidinoneHCID 13872762.2%

반응 단계

A 0° C. suspension of 2-(methylthio)pyrimidin-4(3H)-one (2.0 g, 14.1 mmol) in DMF (40 mL) was treated with solid LiHMDS (3.06 g, 18.3 mmol), followed by methyl iodide (1.14 mL, 18.3 mmol), warmed to RT and stirred overnight. The mixture was quenched with water, extracted with EtOAc (3×) and the combined organics were dried over Na2SO4, concentrated to dryness and purified via silica gel chromatography (EtOAc/Hex) to afford 3-methyl-2-(methylthio)pyrimidin-4(3H)-one (1.37 g, 62%). 1H NMR (400 MHz, DMSO-d6): δ 7.83 (d, J=6.5 Hz, 1H), 6.17 (d, J=6.5 Hz, 1H), 3.39 (s, 3H), 2.54 (s, 3H); MS (ESI) m/z: 157.1 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09181223B2
출처 데이터셋uspto-grants-2015_11
ORD IDord-ba872198cc934377b4d46c19bd45c718
출처 메모uspto-grants-2015_11