IP Library Granted Patent US 8,664,274
Granted Patent B2
US 8,664,274 · App. 13/176,866 · Granted Mar 4, 2014

Sulfonyl semicarbazides, semicarbazides and ureas, pharmaceutical compositions thereof, and methods for treating hemorrhagic fever viruses, including infections associated with arena viruses

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Quick Facts
Patent No.
US 8,664,274
App. No.
13/176,866
Granted
Mar 4, 2014
Kind
B2
Abstract

Compounds, methods and pharmaceutical compositions for treating viral infections, by administering certain novel sulfonyl semicarbazides, carbonyl semicarbazides, semicarbazides, ureas and related compounds in therapeutically effective amounts are disclosed. Methods for preparing the compounds and methods of using the compounds and pharmaceutical compositions thereof are also disclosed. In particular, the treatment and prophylaxis of viral infections such as caused by hemorrhagic fever viruses is disclosed, i.e., including but not limited to, Arenaviridae (Junin, Machupo, Guanarito, Sabia, Lassa, Tacaribe, Pinchinde, and VSV), Filoviridae (ebola and Marburg viruses), Flaviviridae (yellow fever, omsk hemorrhagic fever and Kyasanur Forest disease viruses), and Bunyaviridae (Rift Valley fever).

Claims (27)

1. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a pharmaceutically effective amount of a compound of Formula II:

wherein,

n is an integer from 0-6;

m is an integer from 0-1;

R 1 is selected from the group consisting of H and alkyl;

R 2 is selected from the group consisting of substituted or unsubstituted phenyl, substituted and unsubstituted aryl, substituted and unsubstituted heteroaryl, substituted or unsubstituted alkyl, substituted or unsubstituted branched alkyl, and substituted or unsubstituted unsaturated cycloheteroalkyls;

or where R 1 and R 2 combine together to form a substituted or unsubstituted C 4-10 cyclic saturated heteroalkyl;

R 3 and R 4 are independently selected from the group consisting of H and alkyl;

or a pharmaceutically acceptable salt thereof.

2. The pharmaceutical composition of claim 1 , wherein n is 0, 1, or 2.

3. The pharmaceutical composition of claim 1 , wherein n is 1.

4. The pharmaceutical composition of claim 1 , wherein m is 1.

5. The pharmaceutical composition of claim 1 , wherein m is 1 and n is 1.

6. The pharmaceutical composition of claim 1 , wherein the compound of Formula II is selected from the group consisting of: 2-[2,5-bis(2,2,2-trifluoroethoxy)benzoyl]-N[-][1,1-bis(trifluoromethyl)propyl]hydrazinecarboxamide; N-[1,1-bis(trifluoromethyl)propyl]-2-(4-tert-butylbenzoyl)hydrazinecarboxamide; 2-(1,1′-biphenyl-4-ylcarbonyl)-N-[1,1-bis(trifluoromethyl)propyl]hydrazinecarboxamide; N-[1,1-bis(trifluoromethyl)propyl]-2-(1-naphthoyl)hydrazinecarboxamide; 2-(1,1′-biphenyl-2-ylcarbonyl)-N-[1,1-bis(trifluoromethyl)propyl]hydrazinecarboxamide; N-[1,1-bis(trifluoromethyl)propy 1]-2-(4-methylbenzoyl)hydrazinecarboxamide; N-[1,1-bis(trifluoromethyl)propyl]-2-(2-naphthoyl)drazinecarboxamide; N-[1,1-bis(trifluoromethy[l])propy[1]]-2-(2,5-d[i]methoxybenzoyl)hydrazinecarboxamide; N-[1,1-bis(trifluoromethyl)propyl]-2-(3,4-dichlorobenzoyl)hydrazinecarboxamide; N-[1,1-bis(trifluoromethyl)propy 1]-2-(4-bromobenzoyl)hydrazinecarboxamide; N-[1,1-bis(trifluoromethyl)propyl]-2-(4-isopropylbenzoyl)hydrazinecarboxamide; N-[1,1-bis(trifluoromethyl)propyl]-2-(3,5-dimethylbenzoyl)hydrazinecarboxamide; N-[1,1-bis(trifluoromethyl)propyl]-2-(mesitylcarbonyl)hydrazinecarboxamide; and N-[1,1-bis(trifluoromethyl)propyl]-2-(5-chloro-2-methoxybenzoyl)hydrazinecarboxamide.

7. The pharmaceutical composition of claim 1 , wherein the compound of Formula II is N-[1,1-bis(trifluoromethyl)propyl]-2-(4-methylbenzoyl)hydrazinecarboxamide.

8. The pharmaceutical composition of claim 1 , wherein the compound of Formula II is N-[1,1-bis(trifluoromethyl)propyl]-2-(2,5-dimethoxybenzoyl)hydrazinecarboxamide.

9. The pharmaceutical composition of claim 1 , which further comprises cidofovir, cyclic cidofovir, or salts, esters, or prodrugs thereof.

10. A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a pharmaceutically effective amount of a compound of Formula I:

wherein

n is an integer from 0-6;

m is an integer from 0-1;

p is an integer from 0-1;

R 1 isselected from the group consisting of H and alkyl;

R 2 is selected from the group consisting of substituted or unsubstituted phenyl, substituted and unsubstituted aryl, substituted and unsubstituted heteroaryl, substituted or unsubstituted alkyl, substituted or unsubstituted branched alkyl, and substituted or unsubstituted unsaturated cycloheteroalkyls; or where R 1 and R 2 combine together to form a substituted or unsubstituted C 4-10 cyclic saturated heteroalkyl;

R 3 is selected from the group consisting of H and alkyl;

or a pharmaceutically-acceptable salt thereof,

and further comprising cidofovir, cyclic cidofovir, or salts, esters or prodrugs thereof.

Assignments (6)
RELEASE OF SECURITY INTEREST Recorded Apr 2, 2015
From: GENERAL ELECTRIC CAPITAL CORPORATION, AS AGENT
To: SIGA TECHNOLOGIES, INC.
Reel/Frame 035319/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 22, 2014
From: SIGA TECHNOLOGIES INC.
To: KINETA FOUR LLC
Reel/Frame 033588/0427 →
RELEASE OF SECURITY INTEREST Recorded Aug 14, 2014
From: GENERAL ELECTRIC CAPITAL CORPORATION
To: SIGA TECHNOLOGIES INC.
Reel/Frame 033544/0324 →
SECURITY AGREEMENT Recorded Dec 31, 2012
From: SIGA TECHNOLOGIES, INC.
To: GE CAPITAL EQUITY INVESTMENTS, INC. C/O GE HEALTHCARE FINANCIAL SERVICES, INC.
Reel/Frame 029557/0771 →
CONFIRMATORY LICENSE Recorded Feb 16, 2012
From: SIGA TECHNOLOGIES, INC.
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 027716/0093 →
CONFIRMATORY LICENSE Recorded Dec 12, 2011
From: SIGA TECHNOLOGIES, INC.
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 027364/0451 →