|United States Patent
, et al.
July 23, 2013
Synthesis of azido heterocycles
Energetic candidate azido heterocycles and their synthesis are described.
Duddu; Raja (Hackettstown, NJ), Dave; Paritosh (Bridgewater, NJ), Damavarapu; Reddy (Hackettstown, NJ), Surapaneni; Rao (Long Valley, NJ) |
|Applicant: || |
|Name ||City ||State ||Country ||Type |
The United States of America as Represented by the Secretary of the Army
August 3, 2011|
Related U.S. Patent Documents
||Application Number||Filing Date||Patent Number||Issue Date|
| ||12173883||Jul 16, 2008||8153786|
| ||60949932||Jul 16, 2007|
|Current U.S. Class: ||544/219 |
|Current CPC Class:
||C07D 257/08 (20130101)|
|Current International Class:
||C07D 251/00 (20060101)|
|Field of Search:
References Cited [Referenced By]
U.S. Patent Documents
Primary Examiner: Coleman; Brenda
Attorney, Agent or Firm: Goldfine; Henry S.
FEDERAL INTEREST STATEMENT
The inventions described herein may be manufactured, used and licensed by
the United States Government for United States Government purposes
without payment of any royalties thereon or therefore.
Parent Case Text
CROSS REFERENCE TO RELATED APPLICATION
This application is a divisional application of U.S. patent application
Ser. No. 12/173,883 filed Jul. 16, 2008 now U.S. Pat. No. 8,153,786,
which application claims the benefit of U.S. Provisional Application No.
60/949,932 filed Jul. 16, 2007--the entire file wrapper contents of which
application Ser. No. 12/173,883 and which Provisional Application No.
60/949,932 are both incorporated herein, as if each were set forth in
The invention claimed is:
1. The azido heterocycle tris-triazidomethylmethyloxy triazine.
2. A method of preparing the azido heterocycle compound comprising the steps of: treating cyanuric chloride with stoichiometric amounts of the sodium salt of triazidoalcohol in THF under reflux conditions; and recovering a quantity of
FIELD OF THE INVENTION
This invention relates generally to the field of energetic compounds and in particular to a method for synthesizing azido heterocycles.
BACKGROUND OF THE INVENTION
The synthesis and development of new energetic ingredients have attracted the attention of synthetic organic chemists due to their utility in defense/military applications. Some of the recent examples in this context include
polynitrocyclobutanes,.sup.4 1,3,3, -trinitroazeditine,.sup.5 hexanitrohexaazaisowurtzitane (2,4,6,8,10,12-hexanitro-2,4,6,8,-10,12 hexaazatetracyclo[126.96.36.199.sup.5,9.0.sup.3,11]dodecane (CL-20).sup.6 and octanitrocubane. (See, e.g., Archibald, T. G.;
Garver, L. C.; Baum, K.; Cohen, M. C.; Synthesis of polynitrocyclobutane derivatives. J. Org. Chem., 1989, 54 (12), 2869-2873; Archibald, T. G.; Gilardi, R.; Baum, K.; George, C.; Synthesis and X-ray crystal structure of 1,3,3-trinitroazetidine. J.
Org. Chem., 1990, 55 (9), 2920-2924. b) Axenrod, T.; Watnick, C.; Yazdekhasti, H.; Dave, P. R.; Synthesis of 1,3,3-trinitroazetidine. Tetrahedron Lett., 1993, 34 (42), 6677-6680. c) Katritzky, A. R.; Cundy, D. J.; Chen, J.; Novel syntheses of
1,3,3-trinitroazetidine. J. Heterocyclic Chem., 1994, 31 (2), 271-275. d) Axenrod, T.; Watnick, C.; Yazdekhasti, H.; Dave, P. R.; Synthesis of 1,3,3-trinitroazetidine via the oxidative nitrolysis of N-p-tosyl-3-azetidinone oxime. J. Org. Chem., 1995,
60 (7), 1959-1964. e) Hiskey, M. A.; Coburn; M. Synthesis of 1,3,3-trinitroazetidine. U.S. Pat. No. 5,336,784, Aug. 9, 1994. f) Marchand, A. P.; Rajagopal, D.; Batt, S. G.; Archibald, T. G.; A novel approach to the synthesis of
1,3,3-trinitroazetidine. J. Org. Chem., 1995, 60 (15), 4943-4946. g) Hayashi, K.; Kumagai, T.; Nagao, Y.; Improved synthesis of an energetic material 1,3,3-trinitroazetidine exploiting 1-azabicyclo[1.1.0]butane. Heterocycles. 2000, 53 (2), 447-452.;
Nielsen, A. T.; Chafin, A. P.; Christian, S. L.; Moore, D. W.; Nadler, M. P.; Nissan, R. A.; Vanderah, D. J.; Gilardi, R. D.; George, C. F.; Flippen-Anderson, J. L.; Synthesis of Polyazapoly-cyclic Caged Polynitramines. Tetrahedron, 1998, 54 (31),
11793-11812. b) Duddu, R.; Dave, P. R.; "Processes and compositions for nitration of N-substituted isowurtzitanes." U.S. Pat. No. 6,015,898; Jan. 18, 2000. c) Duddu, R.; Dave, P. R.; "Processes and compositions for nitration of N-substituted
isowurtzitanes." U.S. Pat. No. 6,160,113; Dec. 12, 2000. d) Sysolyatin, S. V.; Lobanova, A. A.; Chemikova, Y. T.; Sakovich, G. V.; Methods of synthesis and properties of hexanitrohexaazaisowurtzitane. Russ. Chem. Rev., Russ. Chem. Rev., 2005,
74(8), 757-764; Zhang, M.; Eaton, P. E.; Gilardi, R.; Hepta- and octanitrocubanes. Angew. Chem. Int. Ed., 2000, 39 (2), 401.
SUMMARY OF THE INVENTION
An advance is made in the art according to the principles of the present invention directed novel heterocyclic compounds containing mono- and poly-azido substitutions and their method of preparation.
More particularly, according to an aspect of the present invention, Azidoacetyl Pentanitrohexaazaisowurtzitane is prepared from Pentanitrohexaazaisowurtzitane, Cyanuric Chloride and Dichlorotetrazine whereby the Pentanitrohexaazaisowurtzitane is
reacted with Chloroacetyl Chloride and the reaction products subsequently treated with Sodium Azide in Acetone under reflux conditions.
According to another aspect of the present invention, tris-triaxidomethylmethyloxy triazine and bis-triazidomethylmethyloxytetrazine are prepared by treating Cyanuric Chloride and Dichlorotetrazine with stoichiometric amounts of the sodium salt
of triazidoalcohol in Tetrahydrofuran (THF) under reflux conditions.
In summary, successful preparation and isolation of azidoacetylpentanitro-hexaazaisowurtzitane (3), tris-(triazidomethyl)methoxytriazine (5), and bis(tri-azidomethyl)methoxytetrazine (7), along with X-ray structural characterization of 5 and 7
BRIEF DESCRIPTION OF THE DRAWING
Further features and advantages of the present invention may be understood from the drawing in which:
FIG. 1 is a reaction scheme for azidoacetyl pentanitrohexaazaisowurtzitane according to an aspect of the present invention;
FIG. 2 is a reaction scheme for tris-triazdomethylmethyloxy triazine (5) and bis-triazidomethylmethyloxytetrazine (7) according to another aspect of the present invention;
FIG. 3 is a view of tris-triazdomethylmethyloxy triazine in which (3A) H atoms and the "B" substituent on the triazine ring are omitted and, (3B) the H atoms and the "C" substituent on the triazine ring are omitted;
FIG. 4 is a view down the b axis of the unit cell of the packing in the crystal of tris-triazdomethylmethyloxy triazine;
FIG. 5 is an ortep view of bis-triazidomethylmethloxytetrazine; and
FIG. 6 is a table showing X-ray structural data for tris-triazdomethylmethyloxy triazine and bis-triazidomethylmethloxytetrazine.
The following merely illustrates the principles of the invention. It will thus be appreciated that those skilled in the art will be able to devise various arrangements which, although not explicitly described or shown herein, embody the
principles of the invention and are included within its spirit and scope.
Furthermore, all examples and conditional language recited herein are principally intended expressly to be only for pedagogical purposes to aid the reader in understanding the principles of the invention and the concepts contributed by the
inventor(s) to furthering the art, and are to be construed as being without limitation to such specifically recited examples and conditions.
Moreover, all statements herein reciting principles, aspects, and embodiments of the invention, as well as specific examples thereof, are intended to encompass both structural and functional equivalents thereof. Additionally, it is intended
that such equivalents include both currently known equivalents as well as equivalents developed in the future, i.e., any elements developed that perform the same function, regardless of structure.
Turning now to FIG. 1, there is shown a reaction scheme for the production of azidoacetyl pentanitrohexaazisowurzitane (3) according to an aspect of the present invention. In particular, pentanitrohexaazaisowurtzitane (1), (See, e.g., Bellamy,
A. J.; 31.sup.st Intl. Annual Conference of ICT, Karlsruhe, Germany, Jun. 27-30, 2000, 109-1 b) Lukyanov, O. A.; Shlykova, N. I.; Pentanitro- and Pentanitroso-2,4,6,8,10,12-hexaazoisowurtzitanes. Russ. Chem. Bull (English)., 2004, 53(3), 539-541 c)
Duddu, R.; Dave, P. R.; Damavarapu, R.; Surapaneni, R.; Gilardi, R.; Hydrogenolytic denitration of polynitro compounds. Syn. Comm., 2005, 35(20), 2709-2714. d) Lukyanov, O. A.; Shlykova, N. I.; Penatnitro- and
pentanitroso-2,4,6,8,10,12-hexazaisowurtzitanes. Russ. Chem. Bull. Int. Ed (Engl. Transl.)., 2004, 53 (3), 566-568.), is reacted with chloroacetyl chloride to produce a corresponding chloro derivative (2) which upon treatment with sodium azide in
acetone under reflux conditions affords azido compound (3).
With reference now to FIG. 2, there is shown a reaction scheme for the production of tris-triazidomethylmethyloxy triazine (5) and bis-triazidomethylmethyloxytetrazine (7) according to another aspect of the present invention. More particularly,
cyanuric chloride (4) and dichlorotetrazine (6) (See, e.g., Chavez, D. E.; Hiskey, M. A.; 1,2,4,5-Tetrazine based energetic materials. J. energetic. materials., 1999, 17, 357) are treated with stoichiometric amounts of the sodium salt of
triazidoalcohol (See, e.g., Dave, P. R.; Duddu, R.; Damavarapu, R.; Gelber, R.; Yang, K.; Surapaneni, C. R.; "Polyazido compounds". U.S. Pat. No. 6,841,690 B1; Jan. 11, 2005. b) Dave, P. R.; Duddu, R. G.; Gelber, N.; Yang, K.; Surapaneni, C. R.;
Preparation of cage molecule based polyazido core units for dendrimer synthesis. Tetrahedron Lett., 2004, 45(10), 2159) in THF under reflux conditions. The products (5) and (7)--after work up--were isolated as solids in 72 and 52% yields respectively.
Their structures were established unambiguously with single crystal X-ray crystallography.
All melting points were recorded by a capillary melting point apparatus and uncorrected. The IR spectra were determined on a Perkin-Elmer FT-IR Spectrum-2000 spectrometer. .sup.1H and .sup.13C NMR spectra were recorded on a Bruker Avance 400
MHz NMR spectrometer with CDCl.sub.3 and acetone-d.sub.6 solvents. The chemical shift values were reported in 8 units (part per million) relative to TMS as an internal standard.
Azidoacetyl pentanitrohexaazaisowurtzitane (3): A mixture of pentanitro-hexaazaisowurtzitane (1.0 gm, 2.54 mmol) and chloroacetyl chloride (5 ml, excess) was heated in a sealed tube at 100.degree. C. for 48 h. The reaction mixture was cooled to
room temperature and evaporated to dryness. The residue was treated with ether, filtered, washed the solid with ether and air dried at room temperature to obtain 3 as a white solid. Yield: (0.98 gm, 82%). m.p: 201-202.degree. C.; IR(KBr): 3040 (s),
1719 (s), 1593 (br, vs), 1325 (br, vs), 1275 (br, vs), 1155 (m), 1045 (m), 940 (s), 877 (s) Cm.sup.-1; .sup.1H NMR (Acetone-d.sub.6): 4.52 (s, 2H), 7.82 (br s, 1H), 7.98 (d AB, J.sub.AB=8.0 Hz, 1H) 8.05 (d, J=8.0 Hz, 1H), 8.22 (d AB, J.sub.AB=8.0 Hz,
1H), 8.28 (br s, 2H); Compound 5 was used as such without any further purification. Thus, the chloroacetyl substrate 5 (238 mg, 0.50 mmol) in acetone (5 mL) was treated with sodium azide (0.65 gm, 10 mmol) and the resulting heterogeneous mixture was
refluxed for 12 h. The reaction mixture was cooled to room temperature and filtered. The filtrate was evaporated and the residue was column chromatographed with si-gel (10% ethyl acetate:hexane as eluting solvent) to afford the product as a white solid. Yield: (214 mg, 88%). m.p: 109-111.degree. C.; IR (KBr): 3040 (m), 2121 (s), 1709 (s), 1595 (vs), 1397 (m), 1267 (br, vs), 1165 (m), 1049 (s) cm.sup.1; .sup.1NMR (Acetone-d.sub.6): 4.34 (s, 2H), 7.81 (br s, 1H), 7.96 (d AB, J.sub.AB=8.0 Hz, 1H), 8.02
(d, J=6.6 Hz, 1H), 8.20 (d AB, J.sub.AB=8.0 Hz, 1H), 8.28 (br s, 2H); .sup.33C NMR (Acetone-d.sub.6): 50.80, 68.59, 71.75 (2C), 71.82, 72.76, 76.04, 166.43.
Tris-triazidomethylmethyloxy triazine (5): A three neck 50 mL round bottom reaction flask equipped with a reflux condenser, magnetic stirring bar and a rubber septum was charged with a 95% NaH (84 mg, 95%, 3.3 mmol) and dry TI-IF (10 mL) under
nitrogen atmosphere. To this resulting suspension was added drop-wise triazidoalcohol (597 mg, 3.03 mmol) in dry THF (5 mL) via syringe. The mixture was stirred in a preheated (80.degree. C.) oil bath for 3 h. The reaction mixture was cooled to room
temperature and was then added in portions cyanuric chloride (184 mg, 1.0 mmol). After complete addition of cyanuric chloride, the reaction mixture was subjected to reflux for 7 days. Reaction mixture was cooled to room temperature and poured over
crushed ice and extracted with ethylacetate (3.times.25 mL). The combined organic layer was washed with water (1.times.30 mL), brine (1.times.30 mL) and dried (Na.sub.2SO.sub.4). Evaporation of the solvent followed by Si-gel column chromatography (5%
EtOAc-Hexane) afforded the pure product as a white solid in 72% (480 mg) yield. m.p.: 74-75.degree. C.; density: 1.473 g/cc (measured by gas pycnometer); IR (KBr): 2933 (s), 2866 (m), 2551 (m), 2527 (m), 2103 (vs), 1731 (m), 1563 (vs), 1448 (vs), 1331
(vs), 1129 (vs) cm.sup.-1; .sup.1H-NMR (CDCl.sub.3): 3.91 (s, 18H, 9xCH.sub.2); .sup.13C-NMR (CDCl.sub.3): .delta.0.76, 85.58, and 170.90.
Bis-triazidomethylmethyloxytetrazine (7): Reaction was carried out following the reaction conditions as mentioned above using dichlorotetrazine (150 mg, 1.0 mmol), triazidoalcohol (396 mg, 2.01 mmol) and sodium hydride (49 mg, 95%, 2.01 mmol) in
THF (15 mL) under reflux for 4 days. The pure product was obtained as a fluorescent pink solid in 52% (245 mg) yield; m.p.: 111-112.degree. C.; IR (KBr): 2927 (w), 2115 (vs), 1695 (br m), 1445 (vs), 1406 (vs), 1303 (s), 1096 (s) 1053 (s)
cm.sup.-11H-NMR (CDCl.sub.3): 3.97 (s, 12H, 6xCH.sub.2); .sup.13C-NMR (CDCl.sub.3): .delta.0.91, 86.05, and 165.28.
Turning now to FIG. 3 there is shown: FIG. 3(A) a view of the tris-triazidomethylmethyloxy triazine (5) omitting H atoms and the "B" substituent on the triazine ring and FIG. 3(B) a view of the tris-triazidomethylmethyloxy triazine (5) omitting
H atoms and the "C" substituent on the triazine ring. The substituents are chemically identical, but display different combinations for the torsional conformations of the azido arms. One purpose of this simplification is to show the substituents
without mutual overlap.
FIG. 4 shows a view down the b axis of the unit cell of the packing in the crystal of tristriazidomethylmethyloxy triazine (5). FIG. 5 shows an Ortep view of the bis-triazidomethylmethyloxytetrazine (6) and FIG. 6 is a table showing X-ray
structural data for the tristriazidomethylmethyloxy triazinec (5) and bis-triazidomethylmethyloxytetrazine (6).
At this point, while we have discussed and described the invention using some specific examples, those skilled in the art will recognize that our teachings are not so limited. For example, the preferred embodiments of the invention have been
provided for the purpose of explaining the principles of the invention and its practical application, thereby enabling others skilled in the art to understand the invention. Various embodiments and various modifications are contemplated. Accordingly,
the invention should be only limited by the scope of the claims attached hereto.
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