Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl chloroformateHCID 10928—
Reactant1-Amino-1H-pyrrole-2-carboxamideHCID 10419180—
Solvent1,4-DioxaneHCID 31275—
ProductPyrrolo[2,1-f][1,2,4]triazine-2,4(1H,3H)-dioneHCID 1560498863%

Reaction Conditions

Temperature155 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534792B2
Source datasetuspto-grants-2009_05
ORD IDord-7346175421b544849ea8be03f9242cb0
Source noteuspto-grants-2009_05