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Reaction of Several Aminopyrimidines With Formaldehyde
Formaldehyde has been shown to react with 2-aminopyrimidine (II) and 2-(methylamino) pyrimidine (V) at room temperature to give the corresponding methylol derivatives or the corresponding methylenebis(aminopyrimidines). The reaction of formaldehyde with 2-amino-4,6-dichloro-5-methylpyrimidine (VII)...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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[Gaithersburg, MD] : U.S. Dept. of Commerce, National Institute of Standards and Technology
1962
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5327744/ http://dx.doi.org/10.6028/jres.066A.007 |
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author | McLeod, Gerald L. |
author_facet | McLeod, Gerald L. |
author_sort | McLeod, Gerald L. |
collection | PubMed |
description | Formaldehyde has been shown to react with 2-aminopyrimidine (II) and 2-(methylamino) pyrimidine (V) at room temperature to give the corresponding methylol derivatives or the corresponding methylenebis(aminopyrimidines). The reaction of formaldehyde with 2-amino-4,6-dichloro-5-methylpyrimidine (VII) and also its failure to react with 2-(dimethylamino)pyrimidine (IX) are cited as evidence that the pyrimidine ring is not involved in the reaction. |
format | Online Article Text |
id | pubmed-5327744 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1962 |
publisher | [Gaithersburg, MD] : U.S. Dept. of Commerce, National Institute of Standards and Technology |
record_format | MEDLINE/PubMed |
spelling | pubmed-53277442023-06-15 Reaction of Several Aminopyrimidines With Formaldehyde McLeod, Gerald L. J Res Natl Bur Stand A Phys Chem Article Formaldehyde has been shown to react with 2-aminopyrimidine (II) and 2-(methylamino) pyrimidine (V) at room temperature to give the corresponding methylol derivatives or the corresponding methylenebis(aminopyrimidines). The reaction of formaldehyde with 2-amino-4,6-dichloro-5-methylpyrimidine (VII) and also its failure to react with 2-(dimethylamino)pyrimidine (IX) are cited as evidence that the pyrimidine ring is not involved in the reaction. [Gaithersburg, MD] : U.S. Dept. of Commerce, National Institute of Standards and Technology 1962 1962-02-01 /pmc/articles/PMC5327744/ http://dx.doi.org/10.6028/jres.066A.007 Text en https://creativecommons.org/publicdomain/zero/1.0/ The Journal of Research of the National Bureau of Standards Section A is a publication of the U.S. Government. The papers are in the public domain and are not subject to copyright in the United States. Articles from J Res may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright. |
spellingShingle | Article McLeod, Gerald L. Reaction of Several Aminopyrimidines With Formaldehyde |
title | Reaction of Several Aminopyrimidines With Formaldehyde |
title_full | Reaction of Several Aminopyrimidines With Formaldehyde |
title_fullStr | Reaction of Several Aminopyrimidines With Formaldehyde |
title_full_unstemmed | Reaction of Several Aminopyrimidines With Formaldehyde |
title_short | Reaction of Several Aminopyrimidines With Formaldehyde |
title_sort | reaction of several aminopyrimidines with formaldehyde |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5327744/ http://dx.doi.org/10.6028/jres.066A.007 |
work_keys_str_mv | AT mcleodgeraldl reactionofseveralaminopyrimidineswithformaldehyde |