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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374685Generated: October 25, 2026

Carbamimidic acid, methyl ester, sulfate (1:1) → 4-(2-Azido-ethoxymethyl)-6-(2-chloro-phenyl)-2-methoxy-1,6-dihydro-pyrimidine-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1374685

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbamimidic acid, methyl ester, sulfate (1:1)HCID 169039—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl (2-Azidoethoxy)aceto-2-(2-chlorophenylmethlene)acetateHCID 71433737—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
Product4-(2-Azido-ethoxymethyl)-6-(2-chloro-phenyl)-2-methoxy-1,6-dihydro-pyrimidine-5-carboxylic acid ethyl esterHCID 178469322—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-[2-(2-azido-ethoxy)-acetyl]-3-(2-chloro-phenyl)-acrylic acid ethyl ester (1.50 g, 4.44 mmol), O-methylisourea sulfate (0.82 g, 6.66 mmol) and sodium bicarbonate (1.5 g, 17.86 mmol) in N,N-dimethylacetamide (25 mL) was heated to 80° C. and maintained at this temperature overnight (ca. 15 h). The mixture was cooled to RT and then taken up in EtOAc (100 mL) and H2O (50 mL). The EtOAc extract was washed with brine (50 mL), dried (Na2SO4), filtered, concentrated and dried in vacuo. The crude product was purified by chromatography using the ISCO Combiflash SQ16× (120 g Redisep silica gel column, 0 to 60% EtOAc in hexanes for 30 min at 40 mL/min) to afford 1.189 g (68% for 2 steps) of white solid as a purified product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166603B2
Source datasetuspto-grants-2007_01
ORD IDord-03754c4907c54f78906b5bdeaf63142d
Source noteuspto-grants-2007_01