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HRID 413472作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Cesium ChlorideHCID 24293—
反応物2-Chloro-3-(chloromethyl)-5-methylpyridineHCID 11206082—
反応物N-nitroimidazolidin-2-imineHCID 135413413—
溶媒AcetonitrileHCID 6342—
生成物1-(2-Chloro-5-methyl-3-pyridylmethyl)2-nitroiminoimidazolidineHCID 13634771290%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06566528B1
出典データセットuspto-grants-2003_05
ORD IDord-7586f01012af4ed18c167210e9a16ebd
出典メモuspto-grants-2003_05