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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2199615생성일: 2026년 10월 26일

Sodium Iodide → HCID 58182714, 화합물

https://huagongshe.com/reaction/2199615

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참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물6-Amino-5-bromopyridine-3-carbonitrileHCID 1491250—
반응물trans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매1,4-DioxaneHCID 31275—
생성물HCID 58182714HCID 58182714—

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온도120 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09359336B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-7e1ee5ac571f4c2ca06910a31bacfc15
출처 메모uspto-grants-2016_06