The hetero ring contains plural nitrogens (e.g., 1,3-diazepines, etc.)

Subclass of:

540 - Organic compounds -- part of the class 532-570 series

540000000 - ORGANIC COMPOUNDS (CLASS 532, SUBCLASS 1)

540001000 - HETEROCYCLIC CARBON COMPOUNDS CONTAINING A HETERO RING HAVING CHALCOGEN (I.E., OXYGEN, SULFUR, SELENIUM OR TELLURIUM) OR NITROGEN AS THE ONLY RING HETERO ATOMS

540484000 - The hetero ring contains seven members including nitrogen and carbon

Patent class list (only not empty are listed)

Deeper subclasses:

Class / Patent application number	Description	Number of patent applications / Date published
540575000	The nitrogens are in the 1,4-positions of the hetero ring	61
540555000	Polycyclo ring system which contains the hetero ring as one of the cyclos	29
540554000	The hetero ring contains at least three nitrogens	4
20080262222	Near infrared dyes - Near infrared (NIR) dyes, image recording substrate including the NIR dye, and methods of making the NIR dyes, are disclosed.	10-23-2008
20140073781	PROCESS FOR OBTAINING A CHARGE OF HEXANITROHEXAAZAISOWURTZITANE CRYSTALS HAVING A ROUNDED MORPHOLOGY; CHARGE AND CORRESPONDING ENERGETIC MATERIAL - The present invention provides a process for obtaining a charge of hexanitrohexaazaisowurtzitane crystals having rounded morphology. It also provides said charge, the energetic material comprising it, and a process for manufacturing said material. Said process for obtaining said charge comprises:	03-13-2014
20140235853	Method of Preparation of epsilon-2,4,6,8,10,12-Hexanitro-2,4,6,8,10,12-Hexaazaisowurtzitane with Reduced Impact Sensitivity - The present invention relates to a method of preparation of ε-2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane with reduced impact sensitivity by precipitation of a solution of 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane in a solvent by an antisolvent, wherein phosphorus(V) oxide is added as a recrystallization promoter to the solution of 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane in the solvent, the obtained mixture is stirred and filtered, and the filtrate is subsequently precipitated by the addition of the antisolvent.	08-21-2014
20150361056	CL-20:DNMT COCRYSTAL CRYSTAL STRUCTURE - A cocrystal of CL-20 (2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane) and DNMT (1-methyl-3,5-dinitro-1,2,4-triazole) was formed through a resonant acoustic mixing process. The resulting cocrystal comprised an essentially 1:1 stoichiometric ratio between these coformers. The cocrystal advantageously has decreased sensitivity when compared with a pure CL-20 sample, and maintains thermal stability and comparable energetic performance.	12-17-2015

Entries
Document	Title	Date
20080319188	Novel pyridine derivatives and pyrimidine derivatives (3) - A compound represented by the following formula, a salt thereof or a hydrate of the foregoing has an excellent hepatocyte growth factor receptor (HGFR) inhibitory activity, and exhibits anti-tumor activity, angiogenesis inhibitory activity and cancer metastasis inhibitory activity.	12-25-2008
20110178292	SYNTHESIS OF CYCLIC AMIDINES - The invention relates to an innovative method for synthesis of cyclic amidines. The synthesis starts from a β-, γ- or δ-lactone which is twofold brominated. After esterification of the carboxyl function, the bromine atoms are nucleophilically substituted and the corresponding diamino compound is obtained. The ring closure to the cyclic amidine is accomplished subsequently by reaction with orthoester, imidate or thioimidate. Owing to interposing additional steps for recovery of the diamino compound in enantiomerically pure form, the enantiomers of the cyclic amidines can be stereoselectively synthesized.	07-21-2011
20140163221	Process for the Synthesis of Cyclic Alkylene Ureas - The invention relates to a process for the synthesis of cyclic alkylene ureas comprising reacting in the presence of a basic catalyst, a difunctional amine A having two primary amino groups, and an aliphatic organic carbonate component C selected from the group consisting of dialkyl carbonates CD and of alkylene carbonates CA, wherein the ratio of the amount of substance Ji(—NH2) of primary amino groups —NH2 in the difunctional amine A to the sum M(C) of the amount of substance n(CD) of carbonate groups of a dialkyl carbonate CD and the amount of substance n(CA) of carbonate groups in an alkylene carbonate CA, is at least more than 2, and to the product obtained by this process.	06-12-2014