HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493129Generated: October 30, 2026
Pyridine → Pyrrolo[2,1-f][1,2,4]triazine-2,4(1H,3H)-dione
https://huagongshe.com/reaction/493129
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 1-Amino-1H-pyrrole-2-carboxamide | HCID 10419180 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Pyrrolo[2,1-f][1,2,4]triazine-2,4(1H,3H)-dione | HCID 15604988 | 63% |
Reaction Steps
Ethyl chloroformate (4.9 ml, 51 mmole) was added dropwise to a stirred mixture of 1-amino-1H-pyrrole-2-carboxamide (5.85 gm, 46.7 mmole, Journal of Heterocyclic Chemistry, 1994, 31, 781) and dry pyridine (4.2 mL, 51 mmole) in dry dioxane (48 mL) under N2 at RT. This was heated at reflux for 1 hr and then the solvent was removed. The residue was heated at 155° C. for 17 hr and then allowed to cool to RT. This was triturated with methanol and the solid was collected by filtration and washed with cold methanol to give the product, 4.43 gm (63% yield): MS: 152 (M+H)+; HPLC Ret Time: 0.36 min (YMC Xterra S7 3.0×50 mm column, 2 min gradient, 5 mL/min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07534792B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-7346175421b544849ea8be03f9242cb0 |
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| Source note | uspto-grants-2009_05 |
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