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HRID 217282생성일: 2026년 10월 24일

Triethylamine → {5-[4-Amino-6-(2-methoxy-phenylsulfanyl)-[1,3,5]triazin-2-yl]-2,4-dichlorophenoxy}-acetonitrile

https://huagongshe.com/ko/reaction/217282

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물ThioguaiacolHCID 23642—
반응물[5-(4-Amino-6-phenylmethanesulfinyl-[1,3,5]triazin-2-yl)-2,4-dichlorophenoxy]-acetonitrileHCID 57898869—
용매DimethylformamideHCID 6228—
생성물{5-[4-Amino-6-(2-methoxy-phenylsulfanyl)-[1,3,5]triazin-2-yl]-2,4-dichlorophenoxy}-acetonitrileHCID 5789881883.3%

반응 단계

Triethylamine (12 μL) and 2-methoxybenzenethiol (12 mg) were added in succession to a solution of the above-described [5-(4-amino-6-phenylmethanesulfinyl-[1,3,5]triazin-2-yl)-2,4-dichlorophenoxy]-acetonitrile (12 mg) in dimethylformamide (0.5 mL). The mixture was stirred at room temperature for 8 hours. After dilution with ethyl acetate (7 mL), the mixture was washed twice with water and once with brine. The mixture was pre-dried over anhydrous sodium sulfate, and filtered. The solvent was distilled off. The resulting residue was purified by silica gel column chromatography (developing solvent: hexane:ethyl acetate=7:3) to give {5-[4-amino-6-(2-methoxy-phenylsulfanyl)-[1,3,5]triazin-2-yl]-2,4-dichlorophenoxy}-acetonitrile as white solid (10 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193351B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-ef965fb2a051411791d949e5a75fcaf6
출처 메모uspto-grants-2012_06