IP Library Granted Patent US 7,674,913
Granted Patent B2
US 7,674,913 · App. 10/514,575 · Granted Mar 9, 2010

Heterocyclic boronic acid compounds

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Quick Facts
Patent No.
US 7,674,913
App. No.
10/514,575
Granted
Mar 9, 2010
Kind
B2
Abstract

Dipeptidyl peptidase IV (DPP-IV)-inhibiting compounds are provided that have formula I: wherein n is 1 to 3; X is CH 2 ; S; O; CF 2 or C(CH 3 ) 2 ; Z is H; halogen; hydroxyl; (C 1-6 )alkoxy; (C 1-12 )alkyl; (C 3-12 )cycloalkyl; phenyl; or heteroaryl; where the phenyl and heteroaryl groups are optionally mono- or independently plurisubstituted with R7; optionally, X together with an adjacent ring carbon and Z form a fused cyclopropyl; and optionally, one of the bonds in the ring containing X is a double bond; and Cr i R ii , R 1 , R 1 , R 3 , R 4 and R 5 are as described herein. Methods for preparing these compounds, and methods for treating diabetes, especially Type II diabetes, and other related diseases are described using the compounds of formula I in pharmaceutical compositions which contain these compounds. Pharmaceutical compositions which contain combinations of these compounds with other antidiabetic agents are also described herein.

Claims (13)

1. A compound of the formula (VI):

or a pharmaceutically acceptable salt thereof, wherein:

R 1 and R 2 independently or together are —OH, a hydroxyl bearing a boronic acid protecting group, or a group capable of being hydrolyzed to a hydroxyl group in an aqueous solution at physiological pH or in biological fluids;

R x is hydrogen, a substituted or unsubstituted C 1-8 alkyl, or a cycloalkyl group; and

the wavy lines at asymmetric carbons C a and C b independently indicate for each asymmetric carbon an R configuration, an S configuration, or a mixture of both configurations.

2. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable carrier.

3. A pharmaceutical combination comprising a compound of any of claim 1 ; and

a second medicament that increases insulin secretion, increases insulin sensitivity, reduces the uptake of sugar from the gastrointestinal track, enhances the effect of endogenous peptides or proteins that affect glycemic control, provides a replacement for endogenous peptides or proteins that affect glycemic control, or any combination thereof.

4. The pharmaceutical combination of claim 3 , wherein the second medicament is glyburide, glipizide, nateglinide, repaglinide, metformin, pioglitazone, rosiglitazone, acarbose, miglitol, exenatide, insulin, glimepiride, glipyride, chlorpropamide, gliclazide, troglitazone, isaglitazone, repaglinide, nateglinide, or a combination thereof.

5. A pharmaceutical combination according to claim 3 wherein the second medicament is an antidiabetic agent.

6. The compound of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

7. The compound of claim 1 , wherein the compound is (2R)-1-{2-[(3R)-pyrrolidin-3-ylamino]-acetyl}-pyrrolidine-2-boronic acid.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 7, 2013
From: PHENOMIX CORPORATION
To: SINO-MED INTERNATIONAL ALLIANCE, INC.
Reel/Frame 031736/0652 →
CORRECTIVE ASSIGNMENT TO REMOVE THE INCORRECT SERIAL NUMBER 10/514,574, RECORDED ON APRIL 8, 2005, REEL 016037, FRAME 0336 Recorded Nov 13, 2008
From: CAMPBELL, DAVID A.; WINN, DAVID; BETANCORT, JUAN M.
To: PHENOMIX CORPORATION
Reel/Frame 021834/0769 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 25, 2005
From: CAMPBELL, DAVID A.; WINN, DAVID; BETANCORT, JUAN M.
To: PHENOMIX CORPORATION
Reel/Frame 016683/0003 →