A one-pot, three-component aminotriazine annulation onto 5-aminopyrazole-4-carbonitriles under microwave irradiation
| dc.contributor.author | Lim, Felicia Phei Lin | |
| dc.contributor.author | Luna, Giuseppe | |
| dc.contributor.author | Dolzhenko, Anton | |
| dc.date.accessioned | 2017-01-30T10:45:57Z | |
| dc.date.available | 2017-01-30T10:45:57Z | |
| dc.date.created | 2015-01-06T20:00:29Z | |
| dc.date.issued | 2015 | |
| dc.identifier.citation | Lim, F.P.L. and Luna, G. and Dolzhenko, A. 2015. A one-pot, three-component aminotriazine annulation onto 5-aminopyrazole-4-carbonitriles under microwave irradiation. Tetrahedron Letters. 56 (3): pp. 521-524. | |
| dc.identifier.uri | http://hdl.handle.net/20.500.11937/5411 | |
| dc.identifier.doi | 10.1016/j.tetlet.2014.12.010 | |
| dc.description.abstract |
A one-pot, three-component, microwave-assisted reaction of 5-aminopyrazole-4-carbonitriles, triethyl orthoformate and cyanamide afforded novel 7-arylamino-substituted 4-aminopyrazolo[1,5-a][1,3,5]triazine-8-carbonitriles. The reaction proceeded in a chemo- and regioselective manner resulting in the successful amino-1,3,5-triazine annulation onto 5-aminopyrazole-4-carbonitriles to give 4-aminopyrazolo[1,5-a][1,3,5]triazine-8-carbonitriles. The operational simplicity of the method and high purity of the products, which can be isolated via simple filtration, make this approach attractive for the preparation of a library of compounds for drug discovery processes. | |
| dc.publisher | Pergamon | |
| dc.subject | Purine isostere | |
| dc.subject | Multicomponent reaction | |
| dc.subject | Microwave-assisted synthesis | |
| dc.subject | Triazine | |
| dc.subject | Pyrazole | |
| dc.title | A one-pot, three-component aminotriazine annulation onto 5-aminopyrazole-4-carbonitriles under microwave irradiation | |
| dc.type | Journal Article | |
| dcterms.source.volume | 56 | |
| dcterms.source.number | 3 | |
| dcterms.source.startPage | 521 | |
| dcterms.source.endPage | 524 | |
| dcterms.source.issn | 0040-4039 | |
| dcterms.source.title | Tetrahedron Letters | |
| curtin.note |
NOTICE: this is the author’s version of a work that was accepted for publication in Tetrahedron Letters. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Tetrahedron Letters, Vol. 56, No. 3 (2015). DOI: 10.1016/j.tetlet.2014.12.010 | |
| curtin.department | School of Pharmacy | |
| curtin.accessStatus | Open access |