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HRID 80236作成日:2026年10月24日

Potassium Phosphate, Tribasic → 1-Benzothiazol-6-yl-3-(4-dimethoxymethyl-pyridin-3-yl)-imidazolidin-2-one

https://huagongshe.com/ja/reaction/80236

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物1-N,2-N-dimethylcyclohexane-1,2-diamineHCID 551074—
反応物3-Bromo-4-(dimethoxymethyl)pyridineHCID 20715145—
反応物1-Benzothiazol-6-yl-imidazolidin-2-oneHCID 66678554—
触媒Copper iodideHCID 83717—
溶媒MethanolHCID 887—
溶媒ChloroformHCID 6212—
溶媒1,4-DioxaneHCID 31275—
生成物1-Benzothiazol-6-yl-3-(4-dimethoxymethyl-pyridin-3-yl)-imidazolidin-2-oneHCID 4987245252.9%

反応手順

Using the same reaction conditions and work up as described in Example 1, step-3,1-benzothiazol-6-yl-imidazolidin-2-one (I-84b: 515 mg, 2.35 mmol) was refluxed with 3-bromo-4-dimethoxymethyl-pyridine (600 mg, 2.584 mmol), copper iodide (44.7 mg, 0.2312 mmol), N,N′-dimethyl-cyclohexane-1,2-diamine (80.8 mg, 0.7405 mmol), potassium phosphate (1.4 g, 7.046 mmol) and 1,4-dioxane (20 mL) at 110° C. for 12 hours to afford the crude product. The reaction was monitored by TLC (10% MeOH in chloroform). Purification by column chromatography on silica gel (2% methanol in chloroform) afforded 460 mg of the product (52.9% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号USRE045173E1
出典データセットuspto-grants-2014_09
ORD IDord-9528f764c4114816a73e1d2b7b3500d0
出典メモuspto-grants-2014_09