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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930494Generated: October 29, 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/930494

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, Intermediate 4 (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 numberUS09296747B1
Source datasetuspto-grants-2016_03
ORD IDord-41e4268a9b5749d69771e0aecb8e8852
Source noteuspto-grants-2016_03