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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619081Generated: October 28, 2026

Guanidine Hydrochloride → 5-(2-Amino-pyrimidin-4-yl)-1H-pyrrole-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/1619081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGuanidine HydrochlorideHCID 5742—
ReactantSodium ethoxideHCID 2723922—
Reactant5-((E)-3-Dimethylamino-acryloyl)-1H-pyrrole-3-carboxylic acid ethyl esterHCID 66678236—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product5-(2-Amino-pyrimidin-4-yl)-1H-pyrrole-3-carboxylic acid ethyl esterHCID 6667829780%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a suspension of 5-((E)-3-Dimethylamino-acryloyl)-1H-pyrrole-3-carboxylic acid ethyl ester (0.25 g, 1.06 mmol) in 4 mL of ethanol, guanidine hydrochloride (0.121 g, 1.27 mmol) and sodium ethylate (0.086 g, 1.27 mmol) were added. The mixture was heated to 110° C. overnight. Then, a further amount of sodium ethylate (0.086 g, 1.27 mmol) was added to the mixture and heating to 115° C. was prolonged for additional 24 hours. The resulting mixture was cooled at room temperature and diluted with water (2 mL). The solid was isolated by filtration, washed with 10 mL of water, dried in a vacuum oven at 40° C. affording to give 0.197 g (80%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772280B2
Source datasetuspto-grants-2014_07
ORD IDord-ec807a6216f546a8bdf60ddc6f805239
Source noteuspto-grants-2014_07