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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | 5-((E)-3-Dimethylamino-acryloyl)-1H-pyrrole-3-carboxylic acid ethyl ester | HCID 66678236 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(2-Amino-pyrimidin-4-yl)-1H-pyrrole-3-carboxylic acid ethyl ester | HCID 66678297 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772280B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-ec807a6216f546a8bdf60ddc6f805239 |
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| Source note | uspto-grants-2014_07 |
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