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Transition metal-free ortho-deuteration of electron-deficient N-heteroarenes
ID
Oražem, Žiga
(
Author
),
ID
Jedlovčnik, Luka
(
Author
),
ID
Birk, Jernej
(
Author
),
ID
Pevec, Andrej
(
Author
),
ID
Jansen-van Vuuren, Ross D.
(
Author
),
ID
Košmrlj, Janez
(
Author
)
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https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.202500667
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Abstract
Selectively deuterated electron-deficient N-containing heteroaromatic systems can enable modulation of metabolism with enhanced therapeutic efficacy in pharmaceuticals and improved properties and stability of functional materials, e.g., imaging dyes, light emitters, and catalysts. Current synthetic approaches to selectively deuterate N-heteroaromatic rings largely rely on transition metal (TM) catalysts, prone to inducing over-deuteration while posing several environmental and sustainability concerns and requiring onerous purification to remove metal traces. In this work, an alternative TM-free approach is reported based on directed ortho metalation, which employs lithium 2,2,6,6-tetramethylpiperidide (LiTMP) such as the base and D$_2$O as a green and accessible electrophilic source of deuterium (D). Since the O-carbamate and carboxamide directing groups (DGs) can be transformed into other functional groups or cross-coupled with aromatic or aliphatic moieties, this enables a modular approach to synthesize a series of drug analogs, as exemplified by the synthesis of a precursor to momelotinib-d$_1$ and the key building block pyrimidine-4-carboxylic-5-d$_1$ acid.
Language:
English
Keywords:
deuteration
,
directed ortho-matalation
,
ortho-deuteration
,
N-heterocycles
,
O-carbamates
,
carboxamides
,
N-heteroarene
,
pyrazine
,
pyridazine
,
pyrimidine
Work type:
Article
Typology:
1.01 - Original Scientific Article
Organization:
FKKT - Faculty of Chemistry and Chemical Technology
Publication status:
Published
Publication version:
Version of Record
Year:
2025
Number of pages:
10 str.
Numbering:
Vol. 28, iss. 42, art. e202500667
PID:
20.500.12556/RUL-173870
UDC:
547.8
ISSN on article:
1434-193X
DOI:
10.1002/ejoc.202500667
COBISS.SI-ID:
247384835
Publication date in RUL:
24.09.2025
Views:
561
Downloads:
317
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Record is a part of a journal
Title:
European journal of organic chemistry
Publisher:
Wiley, Chemistry Europe
ISSN:
1434-193X
COBISS.SI-ID:
18135045
Licences
License:
CC BY 4.0, Creative Commons Attribution 4.0 International
Link:
http://creativecommons.org/licenses/by/4.0/
Description:
This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Secondary language
Language:
Slovenian
Keywords:
devteriranje
,
usmerjeno ortometaliranje
,
ortodevteriranje
,
N-heterocikli
,
O-karbamati
,
karboksamidi
Projects
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
P1-0230
Name:
Organska kemija: sinteza, struktura in aplikacija
Funder:
ARIS - Slovenian Research and Innovation Agency
Project number:
J7-50041
Name:
Razvoj imobiliziranih katalizatorjev za pripravo devteriranih organskih spojin
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