Evidence map›Paper›PMID 34069157›Full record

ArticlePolymers2021

Ureido Functionalization through Amine-Urea Transamidation under Mild Reaction Conditions.

Natalia Guerrero-Alburquerque, Shanyu Zhao, Daniel Rentsch, Matthias M Koebel, Marco Lattuada, Wim J Malfait

Open access · goldAbstract read
In one paragraph

Article in Polymers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 49% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Natalia Guerrero-AlburquerqueLaboratory for Building Energy Materials and Components, Swiss Federal Laboratories for Materials Science and Technology, Empa, Überlandstrasse 129, 8600 Dübendorf, Switzerland.
Shanyu ZhaoLaboratory for Building Energy Materials and Components, Swiss Federal Laboratories for Materials Science and Technology, Empa, Überlandstrasse 129, 8600 Dübendorf, Switzerland.
Daniel RentschLaboratory for Functional Polymers, Swiss Federal Laboratories for Materials Science and Technology, Empa, Überlandstrasse 129, 8600 Dübendorf, Switzerland.ORCID 0000-0002-9335-9527
Matthias M KoebelLaboratory for Building Energy Materials and Components, Swiss Federal Laboratories for Materials Science and Technology, Empa, Überlandstrasse 129, 8600 Dübendorf, Switzerland.
Marco LattuadaDepartment of Chemistry, University of Fribourg, Chemin du Musée 9, 1700 Fribourg, Switzerland.
Wim J MalfaitLaboratory for Building Energy Materials and Components, Swiss Federal Laboratories for Materials Science and Technology, Empa, Überlandstrasse 129, 8600 Dübendorf, Switzerland.
Swiss Federal Laboratories for Materials Science and Technology · CHUniversity of Fribourg · CH

Funding

Swiss National Science Foundation 150638Swiss National Science Foundation 179000
6 · The paper itself

Abstract

Ureido-functionalized compounds play an indispensable role in important biochemical processes, as well as chemical synthesis and production. Isocyanates, and KOCN in particular, are the preferred reagents for the ureido functionalization of amine-bearing compounds. In this study, we evaluate the potential of urea as a reagent to graft ureido groups onto amines at relatively low temperatures (<100 °C) in aqueous media. Urea is an inexpensive, non-toxic and biocompatible potential alternative to KOCN for ureido functionalization. From as early as 1864, urea was the go-to reagent for polyurea polycondensation, before falling into disuse after the advent of isocyanate chemistry. We systematically re-investigate the advantages and disadvantages of urea for amine transamidation. High ureido-functionalization conversion was obtained for a wide range of substrates, including primary and secondary amines and amino acids. Reaction times are nearly independent of substrate and pH, but excess urea is required for practically feasible reaction rates. Near full conversion of amines into ureido can be achieved within 10 h at 90 °C and within 24 h at 80 °C, and much slower reaction rates were determined at lower temperatures. The importance of the urea/amine ratio and the temperature dependence of the reaction rates indicate that urea decomposition into an isocyanic acid or a carbamate intermediate is the rate-limiting step. The presence of water leads to a modest increase in reaction rates, but the full conversion of amino groups into ureido groups is also possible in the absence of water in neat alcohol, consistent with a reaction mechanism mediated by an isocyanic acid intermediate (where the water assists in the proton transfer). Hence, the reaction with urea avoids the use of toxic isocyanate reagents by in situ generation of the reactive isocyanate intermediate, but the requirement to separate the excess urea from the reaction product remains a major disadvantage.

Indexed as

aminecatalystnon-isocyanateureaureaseureido

Identifiers

PMID34069157
PMCPMC8156039
OpenAlexW3163187850

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.