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HRID 2199615作成日:2026年10月27日

Sodium Iodide → 3-Iodo-5-isocyanopyridin-2-amine

https://huagongshe.com/reaction/2199615

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物6-Amino-5-bromopyridine-3-carbonitrileHCID 1491250—
反応物trans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒1,4-DioxaneHCID 31275—
生成物3-Iodo-5-isocyanopyridin-2-amineHCID 58182714—

反応条件

温度120 °C

反応手順

The mixture of 6-amino-5-bromonicotinonitrile (3.315 g, 15.9 mmol, 1 eq), sodium iodide (4.77 g, 2 eq), copper(I) iodide (303 mg, 0.1 eq), and trans-N,N′-dimethylcyclohexane-1,2-diamine (0.52 mL, 0.2 eq) in anhydrous dioxane (40 mL under nitrogen atmosphere was stirred at 120° C. for 20 hours. The mixture was cooled to room temperature then partitioned between ethyl acetate and aqueous ammonium chloride. The organic layer was isolated, further washed with saturated aqueous sodium bicarbonate, brine, and dried with anhydrous sodium sulfate. The upper solution was decanted, concentrated, and the crude solid residue was subject to a column chromatography started first with EtOAc-Hex (1:5 to 1:1) followed by MeOH—CHCl3 (1:100 to 1:20). Product containing fractions were all collected and concentrated. The solid residue was triturated with EtOAc-Hex (1:4) yielding 3-iodo-5-isocyanopyridin-2-amine as an off-white solid in the amount of 2.75 g upon filtration.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09359336B2
出典データセットuspto-grants-2016_06
ORD IDord-7e1ee5ac571f4c2ca06910a31bacfc15
出典メモuspto-grants-2016_06