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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983428Generated: October 25, 2026

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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-1,3,5-triazineHCID 17810—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 3-aminophenylacetateHCID 13054266—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product[3-(4-Chloro-[1,3,5]triazin-2-ylamino)phenyl]acetic acid methyl esterHCID 23536225100%

Reaction Conditions

Temperature0 °C

Reaction Steps

(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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864255B2
Source datasetuspto-grants-2005_03
ORD IDord-170c69d84357419186e64748df4be1f6
Source noteuspto-grants-2005_03