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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1726912생성일: 2026년 10월 27일

Sodium Iodide → {5-[(2-Chloro-5-nitro-phenylamino)-methyl]-2-methylsulfanyl-pyrimidin-4-yl}-methyl-amine

https://huagongshe.com/reaction/1726912

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참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물2-Chloro-5-nitroanilineHCID 22691—
반응물(5-Chloromethyl-2-methylsulfanyl-pyrimidin-4-yl)-methyl-amine hydrochlorideHCID 21988143—
용매AcetonitrileHCID 6342—
생성물{5-[(2-Chloro-5-nitro-phenylamino)-methyl]-2-methylsulfanyl-pyrimidin-4-yl}-methyl-amineHCID 6870028897%

반응 조건

온도0 °C

반응 단계

15.85 g (5-Chloromethyl-2-methylsulfanyl-pyrimidin-4-yl)-methyl-amine hydrochloride, 1.979 g sodium iodide, and 34.49 mL N—N-diisopropylethylamine were solved in 150 ml acetonitrile and cooled to 0° C. 17.085 g 2-Chloro-5-nitro-phenylamine dissolved in 150 ml acetonitrile were added slowly under stirring. The reaction mixture was stirred at room temperature for 48 hrs, then the solvent was evaporated. The residue was solved in a mixture of water/acetic acid ethyl ester (1:1), stirred and the crystalline product was isolated by filtration and dried for 48 h under vacuum at 40° C. The two phases of the mother liquor were separated and the aqueous phase was extracted with dichloromethane. The organic phases were combined, dried over sodium sulfate, the solvent was evaporated and the residue was rubbed with diethyl ether. Both residues were combined and gave of the title product in 97% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07494993B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-c6e4527ee27f491b96e86471f678b9b3
출처 메모uspto-grants-2009_02