A One-Pot Synthesis of Ring-fused 1,3,5-Triazine-2,4(3H)-diones: Reactions with Chlorocarbonyl Isocyanate

DOI: 10.1055/s-1985-31375

Source and publish data:

Synthesis p. 892 - 893 (1985)

Update date:2022-08-03

Topics:

Authors:

Kamal, Ahmed

Sattur, P. B.

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1055/s-1985-31375

Ring-fused 2,4-dioxo-1,2,3,4-tetrahydro-1,3,5-triazines are prepared by cyclocondensation of α-amino-N-heteroarenes with chlorocarbonyl isocyanate in the presence of tertiary amines.

Full text of DOI:10.1055/s-1985-31375

Products guided by the article

Product name:7-Chloro-9-phenyl-1,3,4a,10-tetraaza-phenanthrene-2,4-dione

Cas No:104425-84-5

R&D Labs maybe for 104425-84-5

Shanghai Mintchem Development ., Ltd

Contact:0086 21 5190 8570

Address:R602,4#,89Nong, Mudan Road Pudong Shanghai China
ALPHA PHARMACEUTICAL CO，LTD JIANGSU

Contact:+86-527-84829968,+86-527-84829998

Address:suqian city
LianYunGang Chiral Chemical(CHINA) CO.,LTD

Contact:+86-518-83616958 +86-519-82884848

Address:LianYunGang Chemical Industry Park (JiangSu)
Advanced Biotech

Contact:+1-973-357-0577

Address:10 Taft Rd.
ANTAI BIO-TECH CO LTD

website:http://www.antaibio.com

Contact:0086-21-65663057

Address:Room 2108, Building 2，No. 489 Zhengli Road，200433

Relevant to this article

Lewis acid-catalyzed Meyer-Schuster reactions: methodology for the olefination of aldehydes and ketones

Doi:10.1016/j.tet.2008.02.030
(2008)
On the structures of 5-(4-, 3- and 2-methoxyphenylazo)-3-cyano-1-ethyl-6- hydroxy-4-methyl-2-pyridone: An experimental and theoretical study

Doi:10.1016/j.dyepig.2014.01.007
(2014)
Doi:10.1002/macp.1955.020160113
(1955)
Synthesis and antibacterial properties of new 8-nitrofluoroquinolone derivatives

Doi:10.3390/12061240
(2007)
Novel nucleobase-simplified cyclic ADP-ribose analogue: A concise synthesis and Ca²⁺-mobilizing activity in T-lymphocytes

Doi:10.1039/b925295a
(2010)
Synthesis and mode of action studies of novel {2-(3-R-1H-1,2,4-triazol-5-yl)phenyl}amines to combat pathogenic fungi

Doi:10.1002/ardp.201900092
(2019)

Article Doi