Form vi...

Organic compounds -- part of the class 532-570 series – Organic compounds – Carbohydrates or derivatives

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C514S043000

Reexamination Certificate

active

06482939

ABSTRACT:

BACKGROUND OF THE INVENTION
The present invention relates to a crystalline form of the antiviral compound 5,6-dichloro-2-(isopropylamino)-1-(&bgr;-L-ribofuranosyl)-1H-benzimidazole (also known as 1263W94; the compound of formula (I)), pharmaceutical formulations comprising this crystalline form of the antiviral compound, and their use in therapy.
5,6-Dichloro-2-(isopropylamino)-1-(&bgr;-L-ribofuranosyl)-1H-benzimidazole is a benzimidazole derivative useful in medical therapy. WO96/01833 discloses the compound of formula (I) and its use for the treatment or prophylaxis of viral infections such as those caused by herpes viruses. The compound as disclosed in WO96/01833 is in the form of an amorphous, non-crystalline material.
The structure of 5,6-dichloro-2-(isopropylamino)-1-(&bgr;-L-ribofuranosyl)-1H-benzimidazole, the compound of formula (I), is shown below:
We have now found that the compound of formula (I) can exist in various crystalline forms and solvates. Moreover we have discovered a particular crystalline form of the compound of formula (I) Form VI, which is anhydrous and crystalline and which surprisingly has particularly good pharmaceutical properties. Form VI is the most thermodynamically stable form of the compound of formula (I). It may be easily prepared and may be manufactured on a commercial scale. It is particularly stable and essentially non-hygroscopic. Batches of this crystalline form can be consistently made to a high crystal form purity i.e. where the proportion of other amorphous and crystalline forms of the compound of formula (I) is limited. Furthermore this anhydrous crystalline form has good storage properties and can be readily formulated into pharmaceutical compositions such as tablets and capsules. The crystalline forms and solvates of the compound of formula (I) may be characterized by their X-ray powder diffraction patterns.


REFERENCES:
patent: 3399987 (1968-09-01), Woods et al.
patent: 3555040 (1971-01-01), Frick et al.
patent: 3655901 (1972-04-01), Jensen et al.
patent: 5248672 (1993-09-01), Townsend et al.
patent: 5360795 (1994-11-01), Townsend et al.
patent: 5473063 (1995-12-01), Classon et al.
patent: 5574058 (1996-11-01), Townsend et al.
patent: 5646125 (1997-07-01), Townsend et al.
patent: 5654283 (1997-08-01), Townsend et al.
patent: 5665709 (1997-09-01), Townsend et al.
patent: 6077832 (2000-06-01), Chamberlain et al.
patent: 2319961 (1998-06-01), None
patent: WO 9207867 (1992-05-01), None
patent: WO 9408456 (1994-04-01), None
patent: WO96 01833 (1996-01-01), None
patent: WO97/25337 (1997-07-01), None
patent: WO99/51618 (1999-10-01), None
A. Graul, et al., “1263W94 Antiviral”,Drugs of the Future, vol. 22, No. 7, pp. 707-710 (1997).
Gordon, Irving, et al., “Kinetics of Decay in the Expression of Interferon-Dependent MRNAs Responsible for Resistance to Virus”,Proc. National Academy Sciences USA, vol. 77, No. 1, pp. 452-456 (1980).
Devivar, Rodrigo V., et al., “Benzimidazole Ribonucleosides: Observation of an Unexpected Nitration when Performing Non-Aqueous Diazotizations with t-butyl Nitrite,”Bioorganic & Medicinal Chemistry Letters, vol. 2, No. 9, (1992), pp. 1105-1110.
Tigges, Michael A., et al., “Human CD8+ Herpes Simplex Virus-Specific Cytotoxic T-Lymphocyte Clones Recognize Diverse Viron Protein Antigens”,Journal of Virology, vol. 66, No. 3, (1992), 1622-34.
Devivar, Rodrigo V., et al., “Benzimidazole Ribonucleosides: Design, Synthesis, and Antiviral Activity of Certain 2-(Alkylthio)-and 2-(benzylthio)-5,6-dichloro-1-(B-D-ribofuranosyl) benzimidazoles”,Journal of Medicinal Chemistry, vol. 37, No. 18, (1994), pp. 2942-2949.
Townsend, Leroy B., et al., “Design, Synthesis, and Antiviral Activity Activity of Certain 2,5,6-Trihalo-1-(B-D-ribofuranosyl)benzimidazoles”,Journal of Medicinal Chemistry, vol. 38, No. 20, (1995), 4098-4105.
Yankulov, Krassimir, et al., The Transcriptional Elongation Inhibitor 5,6-Dichloro-1-B-D-ribofuranosylbenzimidazole Inhibits Translation Factor HH-Associated Protein Kinase,Journal of Biological Chemistry, vol. 270, No. 41, (1995), pp. 23922-23925.
Nassiri, M. Reza, et al., “Comparison of Benzimidazole Nucleosides and Ganciclovir on the In Vitro Proliferation and Colony Formation of Human Bone Marrow Progenitor Cells,”British Journal of Haematology, vol. 93, No. 2, (1996), pp. 273-279.
Gudmundsson, Kristjan S., et al., “Synthesis and Antiviral Activity of Certain 5′-Modified Analogs of 2,5,6-Trichloro-1-(B-D-ribofuranosyl) benzimidazole,”Journal of Medicinal Chemistry, vol. 40, No. 5, (1997), pp. 785-793.
Fessenden, Ralph J., et al., “Crystallization”,Organic Laboratory Techniques, 3rdedition, Brooks/Cole (Canada), (2001), only preface and pp. 23-38.
Fieser, Louis D., et al., “Crystallization”,Organic Experiments, DC Heath and Company, Boston, MA, (1964), only preface and pp. 41-51.
Zou, Ruiming, et al., “Design, Synthesis, and Antiviral Evaluation of 2-Chloro-5-6,dihalo-1-(B-D-ribofuranosyl) benzimidazoles as Potential Agents for Human Cytomegalovirus Infections”,Journal of Medicinal Chemistry, vol. 40, No. 5, (1997), pp. 811-818.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Form vi... does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Form vi..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Form vi... will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-2943132

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.