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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632825Generated: October 30, 2026

Carbonic acid-guanidine (1:1) → 6-{2-[(4-Methoxybenzyl)oxy]pyridin-3-yl}-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-2-amine

https://huagongshe.com/reaction/632825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbonic acid-guanidine (1:1)HCID 286947—
ReactantSodium Acetate TrihydrateHCID 23665404—
Reactant3-Dimethylaminomethylene-2'-(4-methoxybenzyloxy)-2,3,5,6-tetrahydro[1,3']bipyridinyl-4-oneHCID 121249582—
SolventEthanolHCID 702—
Product6-{2-[(4-Methoxybenzyl)oxy]pyridin-3-yl}-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-2-amineHCID 121249583—

Reaction Steps

A solution of 3-dimethylaminomethylene-2′-(4-methoxybenzyloxy)-2,3,5,6-tetrahydro[1,3′]bipyridinyl-4-one (673 mg, 1.83 mmol) in ethanol (100 ml) was treated with guanidine carbonate (1.32 g, 7.33 mmol), followed by addition of sodium acetate trihydrate (1.99 g, 14.64 mmol) and the reaction mixture was refluxed for 21 hours. The solvent was removed in vacuo and the residue was partitioned between water and ethyl acetate. The separated organic layer was dried (MgSO4), filtered, and concentrated. Elution through a flash column (silica gel 60, 230-400 mesh, 6% methanol in EtOAc) gave the title compound as a light yellow, amorphous solid (477 mg, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321766B1
Source datasetuspto-grants-2016_04
ORD IDord-1923efe991244fc4821d0d3486214983
Source noteuspto-grants-2016_04