Please use this identifier to cite or link to this item:
https://scholarbank.nus.edu.sg/handle/10635/106405
DC Field | Value | |
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dc.title | Synthesis of new heterocyclic system: 1(5)H-1,5-diazacycl[3.3.2]azine-2,4-dione | |
dc.contributor.author | Dolzhenko, A.V. | |
dc.contributor.author | Dolzhenko, A.V. | |
dc.contributor.author | Chui, W.-K. | |
dc.date.accessioned | 2014-10-29T01:59:32Z | |
dc.date.available | 2014-10-29T01:59:32Z | |
dc.date.issued | 2007-09-01 | |
dc.identifier.citation | Dolzhenko, A.V.,Dolzhenko, A.V.,Chui, W.-K. (2007-09-01). Synthesis of new heterocyclic system: 1(5)H-1,5-diazacycl[3.3.2]azine-2,4-dione. Heterocycles 71 (9) : 2049-2054. ScholarBank@NUS Repository. | |
dc.identifier.issn | 03855414 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/106405 | |
dc.description.abstract | A synthesis of hitherto unknown heterocyclic system 1(5)H-1,5-diazacycl[3.3.2]azine-2,4-dione (5) is presented. The cyclocondensation of 2,6-diaminopyridine (1) with maleic anhydride yielded (5-amino-2-oxo-2,3-dihydroimidazo[1,2-a]pyridin-3-yl)acetic acid (2), which was converted to methyl (5-amino-2-oxo-2,3-dihydroimidazo[1,2-a[pyridin-3-yl) acetate hydrochloride (3). The ester (3) upon treatment with sodium carbonate solution underwent intramolecular cyclization to 2a,3-dihydro-1(5)H-1,5-diazacycl[3.3.2]azine-2,4-dione (4), which was oxidized in alkaline condition to provide 5. © 2007 The Japan Institute of Heterocyclic Chemistry. | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | PHARMACY | |
dc.description.sourcetitle | Heterocycles | |
dc.description.volume | 71 | |
dc.description.issue | 9 | |
dc.description.page | 2049-2054 | |
dc.description.coden | HTCYA | |
dc.identifier.isiut | NOT_IN_WOS | |
Appears in Collections: | Staff Publications |
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