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HRID 217282作成日:2026年10月26日

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

https://huagongshe.com/reaction/217282

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物ThioguaiacolHCID 23642—
反応物[5-(4-Amino-6-phenylmethanesulfinyl-[1,3,5]triazin-2-yl)-2,4-dichlorophenoxy]-acetonitrileHCID 57898869—
溶媒DimethylformamideHCID 6228—
生成物{5-[4-Amino-6-(2-methoxy-phenylsulfanyl)-[1,3,5]triazin-2-yl]-2,4-dichlorophenoxy}-acetonitrileHCID 5789881883.3%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193351B2
出典データセットuspto-grants-2012_06
ORD IDord-ef965fb2a051411791d949e5a75fcaf6
出典メモuspto-grants-2012_06