초록 ▼

The present invention includes a precursor compound pertaining to a 1,2,4-Triazolo[4,3-a][1,3,5]Triazine compound, particularly a 1,2,4-Triazolo[4,3-a][1,3,5]Triazine-3,5,7-Triamine, and novel fused ring structures such as triazolyl-tetrazinyl-aminotriazine compounds, and complexes and salts thereof

The present invention includes a precursor compound pertaining to a 1,2,4-Triazolo[4,3-a][1,3,5]Triazine compound, particularly a 1,2,4-Triazolo[4,3-a][1,3,5]Triazine-3,5,7-Triamine, and novel fused ring structures such as triazolyl-tetrazinyl-aminotriazine compounds, and complexes and salts thereof, and other such chemical structures.

대표청구항 ▼

1. A compound having the chemical formula: wherein R1is --NH2,and R2and R3are independently electron donating groups. 2. The compound of claim 1, wherein R2and R3independently comprise electron donating groups selected from the group consisting of lower alkylamino, diloweralkylamino, amino, ha

1. A compound having the chemical formula: wherein R1is --NH2,and R2and R3are independently electron donating groups. 2. The compound of claim 1, wherein R2and R3independently comprise electron donating groups selected from the group consisting of lower alkylamino, diloweralkylamino, amino, halo, aryl, lower alkoxy, lower aralkoxy, aryloxy, mercapto, and lower alkylthio. 3. The compound of claim 1, wherein R2and R3independently comprise electron donating groups selected from the group consisting of a hydroxyl salt, a carboxyl salt, --ORα,--CRα3,--OCORα,--NRα2,and SRα,where Rαgroup is an alkyl group or. 4. The compound of claim 1, wherein R2and R3independently comprise electron donating groups selected from the group consisting of amino, hydroxy, lower alkoxy, lower alkylamino and diloweralkylamino. 5. The compound of claim of claim 1, wherein either R2or R3comprise --NH2. 6. The compound of claim 1, wherein both R2and R3comprise --NH2. 7. The compound of claim 1, wherein either R2or R3comprise --OCH3. 8. The compound of claim 1, wherein both R2and R3comprise --OCH3. 9. 1,2,4-triazolo[4,3-a][1,3,5]triazine-3,5,7-triamine. 10. A compound comprising separate final product formed from diazotizing the compound of claim 1. 11. The compound of claim 10, wherein the separate final product comprises the chemical structure of: wherein R4is an electron donating group, and R5comprises a third fused ring having greater than five atoms comprising carbon atoms, nitrogen atoms, or a combination thereof. 12. The compound of claim 10, wherein the separate final product comprises chemical compositions for use in a field selected from the group consisting of pharmaceutical, energetic material, colorant, functional fluid, agricultural composition, ultraviolet stabilizer and ultraviolet absorber. 13. The compound of claim 12, wherein the separate final product comprises an energetic material selected from the group consisting of explosive, gas generator, and pyrotechnic. 14. The compound of claim 12, wherein the separate final product comprises an agricultural composition selected from the group consisting of herbicides, pesticides, fungicides and fertilizers. 15. The compound of claim 12, wherein the separate final product comprises a functional fluid. 16. The compound of claim 12, wherein the separate final product comprises a colorant selected from the group consisting of dyes, pigments and indicators. 17. The compound of claim 12, wherein the separate final product comprises a pharmaceutical. 18. A process for the preparation of 1,2,4-triazolo[4,3-a][1,3,5]triazine-3,5,7-substituted, acid salt, comprising the steps of: