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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650621Generated: October 28, 2026

Acetamidine monohydrochloride → Ethyl-2-methyl-4-(2-bromophenyl)-pyrimidine-5-carboxylate

https://huagongshe.com/reaction/650621

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetamidine monohydrochlorideHCID 67170—
ReactantSodium ethoxideHCID 2723922—
Reactant2-(2-Bromo-benzoyl)-3-dimethylamino-acrylic acid ethyl esterHCID 54124011—
SolventEthanolHCID 702—
ProductEthyl-2-methyl-4-(2-bromophenyl)-pyrimidine-5-carboxylateHCID 2283171384%

Reaction Steps

To a fresh prepared solution of sodiumethanolate (prepared from 0.77 g (33.7 mmol) Na in 100 ml Ethanol) 3.18 g (33.7 mmol) acetamidinhydrochloride was added. After 10 Min. a solution of 10.0 g (30.6 mmol) 2-(2-bromo-benzoyl)-3-dimethylamino-acrylic acid ethyl ester in 120 ml ethanol was added and the reaction mixture heated for 16 hrs. at 80°. The solvent was evaporated, the residue distributed between 100 ml H2O and 100 ml CH2Cl2. The aqueous phase was extracted twice with 100 ml CH2Cl2. The combined organic layers were dried (MgSO4), filtrated and evaporated. The residue was purified by chromatography (SiO2, CH2Cl2/MeOH 40:1) to give 8.3 g (84%) 4-(2-bromo-phenyl)-2-methyl-pyrimidine-5-carboxylic acid ethyl ester as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06274588B1
Source datasetuspto-grants-2001_08
ORD IDord-77e26a486be34c55a932310aac681e7c
Source noteuspto-grants-2001_08