Proceedings of the 2017 2nd International Conference on Biological Sciences and Technology (BST 2017)

Synthesis of 4-(4-aminophenoxy)-N-propylpicolinamide

Authors
He-Hua Xiong, Jia Zhi, Yin-Mei Zhuang, Meng-Zi Chen, Yin-Hua Xiong, Qi-Dong Tang
Corresponding Author
He-Hua Xiong
Available Online February 2018.
DOI
https://doi.org/10.2991/bst-17.2018.36How to use a DOI?
Keywords
4-(4-aminophenoxy)-N-propylpicolinamide, Synthesis.
Abstract

4-(4-aminophenoxy)-N-propylpicoliamide 4 is an important intermediate for the synthesis of many biologically active compounds. The compound 4-(4-aminophenoxy)-N-propylpicolinamide was obtained by three simple steps to synthesis from picolinic acid. In this paper, three novel 3-phenyl-1H-pyrazole derivatives were prepared. The structure was confirmed by MS and 1H NMR. Furthermore, the synthetic method was optimized. The total yield of the target product was 80%.

Copyright
© 2018, the Authors. Published by Atlantis Press.
Open Access
This is an open access article distributed under the CC BY-NC license (http://creativecommons.org/licenses/by-nc/4.0/).

Download article (PDF)

Volume Title
Proceedings of the 2017 2nd International Conference on Biological Sciences and Technology (BST 2017)
Series
Advances in Biological Sciences Research
Publication Date
February 2018
ISBN
978-94-6252-472-9
ISSN
2468-5747
DOI
https://doi.org/10.2991/bst-17.2018.36How to use a DOI?
Copyright
© 2018, the Authors. Published by Atlantis Press.
Open Access
This is an open access article distributed under the CC BY-NC license (http://creativecommons.org/licenses/by-nc/4.0/).

Cite this article

TY  - CONF
AU  - He-Hua Xiong
AU  - Jia Zhi
AU  - Yin-Mei Zhuang
AU  - Meng-Zi Chen
AU  - Yin-Hua Xiong
AU  - Qi-Dong Tang
PY  - 2018/02
DA  - 2018/02
TI  - Synthesis of 4-(4-aminophenoxy)-N-propylpicolinamide
BT  - Proceedings of the 2017 2nd International Conference on Biological Sciences and Technology (BST 2017)
PB  - Atlantis Press
SP  - 243
EP  - 246
SN  - 2468-5747
UR  - https://doi.org/10.2991/bst-17.2018.36
DO  - https://doi.org/10.2991/bst-17.2018.36
ID  - Xiong2018/02
ER  -