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HRID 983428作成日:2026年10月26日

2,4-Dichloro-1,3,5-triazine → [3-(4-Chloro-[1,3,5]triazin-2-ylamino)phenyl]acetic acid methyl ester

https://huagongshe.com/reaction/983428

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-Dichloro-1,3,5-triazineHCID 17810—
反応物DiisopropylethylamineHCID 81531—
反応物Methyl 3-aminophenylacetateHCID 13054266—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物[3-(4-Chloro-[1,3,5]triazin-2-ylamino)phenyl]acetic acid methyl esterHCID 23536225100%

反応条件

温度0 °C

反応手順

(3-Amino-phenyl)-acetic acid methyl ester was prepared by reacting 3-aminophenylacetic acid with acetyl chloride in MeOH to afford the corresponding methyl ester, HCl salt, (3.09 g, 15.324 mmol). The ester was dissolved in DMF (5 ml) with DIEA (2.67 ml, 15.324 mmol) and cooled to 0° C. To this solution was added dropwise a 0° C. solution of DMF (5 ml) containing 2,4-dichloro-1,3,5-triazine (2.297 g, 15.324 mmol) and DIEA (2.67 ml, 15.324 mmol). The reaction was stirred at ODC for 15 min and then at RT for 1 h. The reaction mix was diluted with EtOAc and water. The layers were separated, and the aqueous layer was extracted twice with EtOAc. The combined organic layers were washed 4 times with brine and dried over Na2SO4. The crude was concentrated down and dried under reduced pressure, giving [3-(4-chloro-[1,3,5]triazin-2-ylamino)-phenyl]-acetic acid methyl ester (4.3 g, 100%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06864255B2
出典データセットuspto-grants-2005_03
ORD IDord-170c69d84357419186e64748df4be1f6
出典メモuspto-grants-2005_03