戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 730301作成日:2026年10月24日

Iodine → (2,3-Dihydro-benzo[1,4]dioxin-6-yl)-(4-iodo-pyridin-2-yl)-amine

https://huagongshe.com/ja/reaction/730301

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Potassium IodideHCID 4875—
反応物N2-(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-pyridine-2,4-diamineHCID 57808069—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-(4-iodo-pyridin-2-yl)-amineHCID 57808271—

反応条件

温度62.5 °C

反応手順

Isopentyl nitrile (Aldrich Chemical Company) (3.9 mL, 29 mmol) was added to a mixture of N2-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-pyridine-2,4-diamine (Example 2(a), 2.4 g, 9.8 mmol), potassium iodide (Aldrich Chemical Company) (1.6 g, 9.8 mmol), iodine (Aldrich Chemical Company) (1.2 g, 4.9 mmol) and copper (I) iodide (Aldrich Chemical Company) (1.9 g, 9.8 mmol) in 1,2-dimethoxyethane (60 mL). The reaction mixture was heated at 60-65° C. for 1 hr. After cooling to room temperature, the insoluble materials were removed by filtration and the filtrate was diluted with EtOAc, washed with 25% aqueous NH4OH, 5% aqueous sodium bisulfite and then brine. The organic layer was separated, dried over Na2SO4 and concentrated in vacuo. The residue was purified on a Biotage 40 M column (2.5:1 hexane:EtOAc) to give the title compound as an off-white solid. MS (ESI, pos. ion) m/z: 355 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07582657B2
出典データセットuspto-grants-2009_09
ORD IDord-c79233cb225e4a3db5c6eaf432d4190d
出典メモuspto-grants-2009_09