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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 913283Generated: October 31, 2026

5-Aminopyridine-2-carbonitrile → HCID 67390012, compound

https://huagongshe.com/reaction/913283

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Aminopyridine-2-carbonitrileHCID 3871395—
Reactant2-Propanamine, 1-methoxy-, (2S)-HCID 7021536—
ReactantHCID 86646773HCID 86646773—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67390012HCID 67390012—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 2-chloro-4-(2-chloro-4-pyrimidinyl)-1,3,5-triazine (i.e., the product of Example 1, Step B) (100 mg, 0.43 mmol) in tetrahydrofuran (2.0 mL) was added 5-amino-2-pyridinecarbonitrile (86 mg, 0.72 mmol), and the resulting mixture was stirred at 40° C. for 3 h. To this mixture was added (S)-1-methoxy-2-propylamine (0.2 mL), and the resulting mixture was refluxed for 2 h. The solution was concentrated and purified using column chromatography on silica gel eluted with a gradient of 70% to 80% ethyl acetate in hexanes to give 84 mg of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026359B2
Source datasetuspto-grants-2011_09
ORD IDord-aa7ac8d227f345faa9e9716a42e2683e
Source noteuspto-grants-2011_09