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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 413472생성일: 2026년 10월 23일

Potassium Carbonate → 1-(2-Chloro-5-methyl-3-pyridylmethyl)2-nitroiminoimidazolidine

https://huagongshe.com/ko/reaction/413472

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Cesium ChlorideHCID 24293—
반응물2-Chloro-3-(chloromethyl)-5-methylpyridineHCID 11206082—
반응물N-nitroimidazolidin-2-imineHCID 135413413—
용매AcetonitrileHCID 6342—
생성물1-(2-Chloro-5-methyl-3-pyridylmethyl)2-nitroiminoimidazolidineHCID 13634771290%

반응 단계

2-chloro-3-chloromethyl-5-methylpyridine (1.3 g, 0.0076 moles) was added to a well-stirred material comprising of 2-nitroimino-1, 3-diazacyclopentane (1.18 g, 0.00912 moles), potassium carbonate (1.16 g, 0.0083 moles), cesium chloride (0.04 g, 0.00024 moles) in acetonitrile (10 ml) solvent at room temperature. The reaction mixture was refluxed for 5 hours. Solvent was removed under reduced pressure and the mass diluted with water (25 ml). The mass was then extracted with methylene chloride (2×50 ml) and the layers were separated. Organic layer was dried over sodium sulphate and solvent removed under reduced pressure. The residue obtained was subjected to chromatographic purification on silica gel to give 1-(2-chloro-5-methyl-3-pyridylmethyl)-2-nitroiminoimidazolidine in 90% yield. NMR (CDCl3+DMSO d6): δ2.38 (s, 3H, CH3), 3.58 (t, 2H, N—CH2), 3.74 (t, 2H, N—CH2), 4.52 (s, 2H, CH2), 7.54 (s, 1H, aromatic), 812 (s, 1H, aromatic), 8.86 (1H, NH). Mass: M+. 269.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06566528B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-7586f01012af4ed18c167210e9a16ebd
출처 메모uspto-grants-2003_05