HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284698Generated: October 30, 2026
4-Aminopyridine → Ethyl 4-(propylamino)-2-(3-(pyridin-4-yl)ureido)pyrimidine-5-carboxylate
https://huagongshe.com/reaction/2284698
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Aminopyridine | HCID 1727 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl 2-((phenoxycarbonyl)amino)-4-(propylamino)pyrimidine-5-carboxylate | HCID 90052190 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 4-(propylamino)-2-(3-(pyridin-4-yl)ureido)pyrimidine-5-carboxylate | HCID 90053314 | 28.7% |
Reaction Steps
To ethyl 2-((phenoxycarbonyl)amino)-4-(propylamino)pyrimidine-5-carboxylate (E7, 2.89 g) and 4-aminopyridine (3.16 g), N,N-dimethylformamide (30 mL) was added at room temperature, and the mixture was stirred at 70° C. for 30 minutes. The reaction mixture was cooled to room temperature, and then the reaction mixture was poured into water (300 mL). The solid matter was taken by filtration, and purified by silica gel column chromatography (eluent, ethyl acetate) to obtain ethyl 4-(propylamino)-2-(3-(pyridin-4-yl)ureido)pyrimidine-5-carboxylate (E8, 830 mg) as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145415B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-81994395a7104e35a615ea6d15c1e6d5 |
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| Source note | uspto-grants-2015_09 |
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