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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948837Generated: October 31, 2026

Water → 5-(2-Amino-pyrimidin-4-yl)-2-(2,4-dichloro-phenyl)-1h-pyrrole-3-carbonitrile

https://huagongshe.com/reaction/1948837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCarbonic acid-guanidine (1:1)HCID 286947—
Reactant2-(2,4-Dichloro-phenyl)-5-((e)-3-dimethylamino-acryloyl)-1h-pyrrole-3-carbonitrileHCID 46221556—
SolventDimethylformamideHCID 6228—
Product5-(2-Amino-pyrimidin-4-yl)-2-(2,4-dichloro-phenyl)-1h-pyrrole-3-carbonitrileHCID 4425134783%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a suspension of 2-(2,4-dichloro-phenyl)-5-((E)-3-dimethylamino-acryloyl)-1H-pyrrole-3-carbonitrile (6.80 g, 20.35 mmol) in 82 mL of N,N-dimethylformamide was added guanidine carbonate (9.17 g, 101.75 mmol). The mixture was heated to 110° C. for 18 hours under efficient stirring. Then, a further amount of guanidine carbonate (1.83 g; 20.35 mmol) was added to the mixture and heating to 115° C. was prolonged for additional 22 hours. The resulting mixture was diluted by dropwise addition of 325 mL of water over 30 minutes. The solid was isolated by filtration, washed with 100 mL of water, dried in the air and, finally, in a vacuum oven at 60° C. affording 5.58 g of product as a light brown powder. Yield=83%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399668B2
Source datasetuspto-grants-2013_03
ORD IDord-86ad13a40015422799eb249c7800c0e3
Source noteuspto-grants-2013_03