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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887704Generated: November 2, 2026

1,2-Dichloroethane → 4-amino-N-methylpyrimidine-5-carboxamide

https://huagongshe.com/reaction/1887704

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Aminopyrimidine-5-carboxylic acidHCID 1201440—
ReactantMethylamine hydrochlorideHCID 6364545—
SolventDimethylformamideHCID 6228—
Product4-amino-N-methylpyrimidine-5-carboxamideHCID 1346843885.5%

Reaction Steps

To the mixture of 4-aminopyrimidine-5-carboxylic acid (0.75 g, 5.39 mmol), methylamine hydrogen chloride (0.44 g, 1.2 eq), EDC (1.67 g, 1.5 eq), HOBt (0.87 g, 1.2 eq) in DMF (20 mL) was added DIEA (3.8 mL, 4.0 eq). The mixture was stirred at room temperature overnight. The crude was concentrated and dissolved in EtOAc. It was washed with saturated NaHCO3 solution. The solvent was removed and the crude was purified by silica gel chromatography (0%˜20% MeOH/DCM) to obtain the desired product 4-amino-N-methylpyrimidine-5-carboxamide (0.701 g, isolated yield 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501763B2
Source datasetuspto-grants-2013_08
ORD IDord-4fbe223b193d407082a56e5b2ff038b2
Source noteuspto-grants-2013_08