戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 80235作成日:2026年10月25日

1,4-Dioxane → 1-Benzothiazol-6-yl-3-(4-pyrrolidin-1-ylmethyl-pyridin-3-yl)-imidazolidin-2-one

https://huagongshe.com/reaction/80235

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DioxaneHCID 31275—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物1-N,2-N-dimethylcyclohexane-1,2-diamineHCID 551074—
反応物1-Benzothiazol-6-yl-imidazolidin-2-oneHCID 66678554—
触媒Copper iodideHCID 83717—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物1-Benzothiazol-6-yl-3-(4-pyrrolidin-1-ylmethyl-pyridin-3-yl)-imidazolidin-2-oneHCID 4987265118.9%

反応手順

Using the same reaction conditions and work up as described in Example 1, step -3,3-bromo-4-pyrrolidin-1-ylmethyl-pyridine (I-176a: 290 mg, 1.205 mmol) was refluxed with 1-benzothiazol-6-yl-imidazolidin-2-one (I-84b: 220 mg, 1.004 mmol), copper iodide (19 mg, 0.1004 mmol), N,N′-Dimethyl-cyclohexane-1,2-diamine (42.7 mg, 0.301 mmol), potassium phosphate (640 mg, 3.012 mmol) and 1,4-dioxane (15 mL) at 120° C. for 12 hours to afford the crude product. The reaction was monitored by TLC (5% MeOH in DCM). Purification by column chromatography on silica gel (5% MeOH in chloroform) followed by preparative HPLC afforded 72 mg of the product (18.9% 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-3096c593b7704a7dbfc86954866657e1
出典メモuspto-grants-2014_09