돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 983428생성일: 2026년 10월 25일

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

반응식

참여 물질

역할이름HCID투입량
반응물2,4-Dichloro-1,3,5-triazineHCID 17810—
반응물DiisopropylethylamineHCID 81531—
반응물Methyl 3-aminophenylacetateHCID 13054266—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물[3-(4-Chloro-[1,3,5]triazin-2-ylamino)phenyl]acetic acid methyl esterHCID 23536225100%

반응 조건

온도0 °C

반응 단계

(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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06864255B2
출처 데이터셋uspto-grants-2005_03
ORD IDord-170c69d84357419186e64748df4be1f6
출처 메모uspto-grants-2005_03