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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983547Generated: October 30, 2026

Imidazole → 2-[(2-cyanoethyl)[2-(1H-imidazol-1-yl)-6-methyl-4-pyrimidinyl]amino]acetic acid, ethyl ester

https://huagongshe.com/reaction/983547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(2-Cyanoethyl)glycine ethyl esterHCID 521172—
Reactant4-Chloro-2-methanesulfonyl-6-methylpyrimidineHCID 12397672—
SolventDimethyl SulfoxideHCID 679—
Product2-[(2-cyanoethyl)[2-(1H-imidazol-1-yl)-6-methyl-4-pyrimidinyl]amino]acetic acid, ethyl esterHCID 8658633834.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

To N-cyanoethylglycine, ethyl ester (15.9 g, 102 mmol) (a compound of formula (Y2)) dissolved in DMSO (70 mL) was added 4-chloro-6-methyl-2-methylsulfonylpyrimidine (18.8 g, 91 mmol) (a compound of formula (Y1)) and diisopropylethylamine (18 mL, 100 mmol). After stirring for 16 hours, the reaction temperature was raised to 70° C. and imidazole (26.5 g, 0.39 mol) was added. After stirring for 1 day, the reaction was cooled to ambient temperature and added to ice water. The solid that formed was suction filtered and collected on paper to give 9.9 g of 2-[(2-cyanoethyl)[2-(1H-imidazol-1-yl)-6-methyl-4-pyrimidinyl]amino]acetic acid, ethyl ester (a compound of formula (Yc1)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864263B2
Source datasetuspto-grants-2005_03
ORD IDord-013c41ce8b3a4e0bb2ad8724a41753e8
Source noteuspto-grants-2005_03