Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2384527Generated: November 1, 2026

Pyridine → Pyrrolo[2,1-f][1,2,4]triazine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/2384527

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 numberUS08263765B2
Source datasetuspto-grants-2012_09
ORD IDord-a7ef9e29da9a40fa9cd9803d5e640b21
Source noteuspto-grants-2012_09