Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338697Generated: October 28, 2026

Carbonic acid-guanidine (1:1) → tert-butyl 2-amino-5H,6H,7H,8H-pyrido[4,3-d]pyrimidine-6-carboxylate

https://huagongshe.com/reaction/338697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbonic acid-guanidine (1:1)HCID 286947—
ReactantSodium Acetate TrihydrateHCID 23665404—
Reactanttert-butyl 3-[(dimethylamino)methylene]-4-oxotetrahydro-1(2H)-pyridinecarboxylateHCID 53395404—
SolventMethanolHCID 887—
Producttert-butyl 2-amino-5H,6H,7H,8H-pyrido[4,3-d]pyrimidine-6-carboxylateHCID 2918411855%

Reaction Steps

A solution of 1-t-Butoxycarbonyl-3-(dimethylamino)methylene-4-piperidone (7.64 g, 30.04 mmol) in methanol (190 mL) was treated with guanidine carbonate (21.65 g, 120.16 mmol), followed by sodium acetate trihydrate (32.70 g, 240.32 mmol). The reaction mixture was heated at reflux for 17 hours and the solvent was removed in vacuo. The residue was diluted with water and the mixture was swirled for a few minutes. The undissolved white solid was collected and washed with water, followed by a small amount of cold ethyl acetate to give the title compound (4.10 g, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889870B2
Source datasetuspto-grants-2014_11
ORD IDord-c72e1d7310da47a4a2ee122c2c561eb9
Source noteuspto-grants-2014_11