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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1865905Generated: October 25, 2026

2-Aminopyridine → 6-Amino-4-(2-furyl)-N-(2-pyridyl)-1H-pyrazolo[3,4-d]pyrimidin-1-ylacetamide

https://huagongshe.com/reaction/1865905

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Reactant6-Amino-4-(2-furyl)-1H-pyrazolo[3,4-d]pyrimidin-1-ylacetic acidHCID 22015531—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product6-Amino-4-(2-furyl)-N-(2-pyridyl)-1H-pyrazolo[3,4-d]pyrimidin-1-ylacetamideHCID 2354689372.4%

Reaction Steps

A solution of 6-amino-4-(2-furyl)-1H-pyrazolo[3,4-d]pyrimidin-1-ylacetic acid (200 mg, 0.77 mmol) in DMF (3 mL) was treated with carbonyl diimidazole (125 mg, 0.77 mmol), stirred at room temperature for 2 h, treated with 2-aminopyridine (72 mg, 0.77 mmol), heated to 50° C. for 3 h, cooled and diluted with water. The resulting white solid was filtered, suspended in MeOH, treated with HCl in dioxan (4-M, 1 mL) diluted with diethyl ether and filtered to give the title compound (187 mg, 59%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07629349B2
Source datasetuspto-grants-2009_12
ORD IDord-28f3659d05ae473f85bdaab236f584c2
Source noteuspto-grants-2009_12