IP Library Granted Patent US 10,772,858
Granted Patent B2
US 10,772,858 · App. 15/570,969 · Granted Sep 15, 2020

Benzhydrol derivatives for the management of conditions related to hypoxia inducible factors

Inventors: Binghe Wang (Marietta, GA); Erwin Van Meir (Tucker, GA); Jalisa Holmes Ferguson (Chamblee, GA); Stefan Kaluz (Atlanta, GA); Xingyue Ji (Atlanta, GA)
Assignees: GEORGIA STATE UNIVERSITY RESEARCH FOUNDATION, INC.; EMORY UNIVERSITY
A61K31/192A01N31/04A61K31/085A61K31/09A61K31/166A61K31/17A61K31/175A61K31/341A61K31/343A61K31/351A61K31/352A61K31/357A61K31/381A61K31/397A61K31/40A61K31/421A61K31/435A61K31/436A61K31/443A61K31/444A61K31/445A61K31/475A61K31/495A61K31/536A61K31/538A61K31/5375A61K31/7068A61K45/06A61P35/00C07C43/295C07D205/04C07D207/12C07D211/46C07D213/65C07D263/32C07D265/36C07D295/096C07D307/12C07D307/20C07D307/79C07D309/10C07D311/70C07D319/16C07D333/54C07D405/12C07D491/052
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Quick Facts
Patent No.
US 10,772,858
App. No.
15/570,969
Granted
Sep 15, 2020
Kind
B2
Abstract

This disclosure relates to benzhydrol derivatives for managing conditions related to the Hypoxia Inducible Factor (HIF) pathway such as uses in treating cancer. In certain embodiment, the disclosure contemplates compounds and pharmaceutical compositions. In certain embodiment, the disclosure contemplates compounds disclosed herein as prodrugs, optionally substituted with one or more substituents, derivatives, or salts thereof.

Claims (30)

1. A compound having Formula I

or pharmaceutically acceptable salts thereof, wherein:

A is an aryl ring;

n is 1, 2, or 3;

R 4 and R 7 are each, individually and independently, hydrogen, alkyl, halogen, nitro, cyano, hydroxy, amino, mercapto, formyl, carboxy, carbamoyl, alkoxy, hydroxyalkyl, alkylthio, thioalkyl, alkylamino, aminoalkyl, (alkyl) 2 amino, alkanoyl, alkoxycarbonyl, alkylsulfinyl, alkylsulfonyl, arylsulfonyl, carbocyclyl, aryl, or heterocyclyl;

R 5 and R 6 are each alkoxy;

R 9 is alkoxy substituted with R 20 ;

R 20 is carbocyclyl, aryl, or heterocyclyl, wherein R 20 is substituted with one or more, the same or different, R 21 ; and

R 21 is halogen, nitro, cyano, hydroxy, trifluoromethoxy, trifluoromethyl, amino, formyl, carboxy, carbamoyl, mercapto, sulfamoyl, methyl, ethyl, methoxy, ethoxy, isopropoxy, tert-butoxy, hydoxymethyl, hydroxyethyl, thiomethyl, thioethyl, aminomethyl, aminoethyl, acetyl, acetoxy, methylamino, ethylamino, dimethylamino, diethylamino, N-methyl-N-ethylamino, acetylamino, N-methylcarbamoyl, N-ethylcarbamoyl, N,N-dimethylcarbamoyl, N,N-diethylcarbamoyl, N-methyl-N-ethylcarbamoyl, methylthio, ethylthio, methylsulfinyl, ethylsulfinyl, mesyl, ethylsulfonyl, methoxycarbonyl, ethoxycarbonyl, isopropoxycarbonyl, tert-butoxycarbonyl, N-methylsulfamoyl, N-ethylsulfamoyl, N,N-dimethylsulfamoyl, N,N-diethylsulfamoyl, N-methyl-N-ethylsulfamoyl, carbocyclyl, aryl, or heterocyclyl.

2. The compound according to claim 1 , wherein A is phenyl.

3. The compound according to claim 1 , wherein R 9 is (2-piperidin-4-yl)ethoxy or (2-(N-alkoxycarbonyl)piperidin-4-yl)ethoxy.

4. A compound having Formula II

or pharmaceutically acceptable salts thereof wherein,

X is —CH 2 O— or —CH 2 CH 2 O—;

R 12 is carbocyclyl, aryl, or heterocyclyl, wherein R 12 is substituted with one or more, the same or different, R 20 ;

R 20 is alkyl, halogen, nitro, cyano, hydroxy, amino, mercapto, formyl, carboxy, carbamoyl, hydroxyalkyl, alkoxy, thioalkyl, alkylthio, aminoalkyl, alkylamino, (alkyl) 2 amino, alkanoyl, alkoxycarbonyl, alkylsulfinyl, alkylsulfonyl, arylsulfonyl, carbocyclyl, aryl, or heterocyclyl, wherein R 20 is optionally substituted with one or more, the same or different, R 21 ;

R 21 is halogen, nitro, cyano, hydroxy, trifluoromethoxy, trifluoromethyl, amino, formyl, carboxy, carbamoyl, mercapto, sulfamoyl, methyl, ethyl, methoxy, ethoxy, isopropoxy, tert-butoxy, hydoxymethyl, hydroxyethyl, thiomethyl, thioethyl, aminomethyl, aminoethyl, acetyl, acetoxy, methylamino, ethylamino, dimethylamino, diethylamino, N-methyl-N-ethylamino, acetylamino, N-methylcarbamoyl, N-ethylcarbamoyl, N,N-dimethylcarbamoyl, N,N-diethylcarbamoyl, N-methyl-N-ethylcarbamoyl, methylthio, ethylthio, methylsulfinyl, ethylsulfinyl, mesyl, ethylsulfonyl, methoxycarbonyl, ethoxycarbonyl, isopropoxycarbonyl, tert-butoxycarbonyl, N-methylsulfamoyl, N-ethylsulfamoyl, N,N-dimethylsulfamoyl, N,N-diethylsulfamoyl, N-methyl-N-ethylsulfamoyl, carbocyclyl, aryl, or heterocyclyl;

R 2 is hydrogen, alkyl, halogen, or alkoxy;

R 3 is hydrogen, alkyl, halogen, or alkoxy;

R 4 , R 7 , and R 8 are each hydrogen;

R 10 is alkyl, formyl, alkanoyl, carbamoyl, hydroxyalkyl, aminoalkyl, or thioalkyl wherein R 10 is optionally substituted with one or more, the same or different, R 20 ; and

R 15 is alkyl, formyl, alkanoyl, carbamoyl, hydroxyalkyl, aminoalkyl, or thioalkyl wherein R 5 is optionally substituted with one or more, the same or different, R 20 .

5. The compound according to claim 4 , wherein X is —CH 2 CH 2 O—.

6. The compound according to claim 5 , wherein R 12 is heterocyclyl.

7. The compound according to claim 1 , selected from the group consisting of

tert-butyl 4-(2-(4-(hydroxy(3,4-dimethoxyphenyl)methyl)-3-methylphenoxy)ethyl)piperidine-1-carboxylate; and

tert-butyl 4-(2-(4-(hydroxy(3, 4,5-trimethoxyphenyl)methyl)-3-methylphenoxy)ethyl)piperidine-1-carboxylate.

8. A pharmaceutical composition, comprising a compound according to claim 1 , or a pharmaceutically acceptable salt and a pharmaceutically acceptable excipient.

9. The compound according to claim 1 , wherein R 9 is ((piperidin-4-yl)oxy)methyl.

10. The compound according to claim 1 , wherein the compound is tert-butyl 4-(2-(4-(hydroxy(3,4-dimethoxyphenyl)methyl)-3-methylphenoxy)ethyl)piperidine-1-carboxylate.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 1, 2020
From: VAN MEIR, ERWIN; KALUZ, STEFAN
To: EMORY UNIVERSITY
Reel/Frame 052801/0496 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 1, 2020
From: WANG, BINGHE; FERGUSON, JALISA HOLMES; JI, XINGYUE
To: GEORGIA STATE UNIVERSITY RESEARCH FOUNDATION, INC.
Reel/Frame 052801/0556 →
CONFIRMATORY LICENSE Recorded Jan 26, 2018
From: EMORY UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 045165/0977 →
Continuity (2)
Provisional Application 62155501 · May 1, 2015
Related Publication 20180289664A1 · Oct 11, 2018