Evidence map›Paper›PMID 35497585›Full record

ArticleRSC advances2020

Microwave-assisted simple synthesis of 2-anilinopyrimidines by the reaction of 2-chloro-4,6-dimethylpyrimidine with aniline derivatives.

Cristina Campestre, György Keglevich, János Kóti, Luca Scotti, Carla Gasbarri, Guido Angelini

Abstract read
In one paragraph

Article in RSC advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Cristina CampestreDepartment of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara via dei Vestini 66100 Chieti Italy guido.angelini@unich.it +39-0871-3554785.ORCID https://orcid.org/0000-0001-5870-7509
György KeglevichDepartment of Organic Chemistry and Technology, Budapest University of Technology and Economics 1521 Budapest Hungary.ORCID https://orcid.org/0000-0002-5366-472X
János KótiSpectroscopic Research Division, Gedeon Richter Plc. 1475 Budapest Hungary.
Luca ScottiDepartment of Medical, Oral and Biotechnological Sciences, University "G. d'Annunzio" of Chieti-Pescara via dei Vestini 66100 Chieti Italy.ORCID https://orcid.org/0000-0003-2662-8720
Carla GasbarriDepartment of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara via dei Vestini 66100 Chieti Italy guido.angelini@unich.it +39-0871-3554785.ORCID https://orcid.org/0000-0002-2236-8733
Guido AngeliniDepartment of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara via dei Vestini 66100 Chieti Italy guido.angelini@unich.it +39-0871-3554785.ORCID https://orcid.org/0000-0001-8353-4590

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A series of 2-anilinopyrimidines including novel derivatives has been obtained from 2-chloro-4,6-dimethylpyrimidine by aromatic nucleophilic substitution with differently substituted anilines under microwave conditions. The substituents had a significant impact on the course and efficiency of the reaction. The results reported herein demonstrate the efficacy of microwaves in the synthesis of the title heterocyclic compounds as compared to the results obtained with conventional heating. The 2-anilinopyrimidines described are of potential bioactivity.

Identifiers

PMID35497585
PMCPMC9050660

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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.