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Benzamide derivatives as modulators of the follicle stimulating hormone

a technology of follicle stimulating hormone and derivatives, which is applied in the direction of sexual disorder, drug composition, veterinary instruments, etc., can solve the problems of high cost, limited use of fsh, and high cost of oral dosing, and achieve the effect of high cos

Inactive Publication Date: 2016-05-19
MERCK PATENT GMBH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the use of FSH is limited by its high cost, lack of oral dosing, and need of extensive monitoring by specialist physicians.

Method used

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  • Benzamide derivatives as modulators of the follicle stimulating hormone
  • Benzamide derivatives as modulators of the follicle stimulating hormone
  • Benzamide derivatives as modulators of the follicle stimulating hormone

Examples

Experimental program
Comparison scheme
Effect test

example 1

Synthetic Route Towards 2-cyclopropyl-oxazole-4-carboxylic acid [4-chloro-5-[3-(2-oxo-pyrrolidin-1-yl)propylcarbamoyl]-2-(4-o-tolyl-piperazin-1-yl)-phenyl]-amide (1i)

[0219]

[0220]Step 1: 2-Chloro-4-fluoro-benzoic acid 1a (5.0 g, 28.64 mmol) was taken in sulphuric acid (20.0 mL) and cooled to 0° C. Nitric acid (10.0 ml) was added to this very carefully and slowly. The reaction was stirred at 0-25° C. for 6 h. The white solid was filtered and washed with water and dried at 40° C. under vacuum and used in the next step.

[0221]Step 2: To a solution of 2-chloro-4-fluoro-5-nitro-benzoic acid 1b (2.0 g, 9.1 mmol) in DMF (20.0 mL) was added potassium carbonate (2.51 g, 18.21 mmol) slowly followed by 1-o-tolyl-piperazine 1e (1.9 g, 10.93 mmol) and the reaction was stirred at room temperature for 16 h. Water was added carefully and the solution was acidified to pH 5.0 using 1N HCl to give yellow solid which was filtered and dried.

[0222]Step 3: To a solution of 2-chloro-5-nitro-4-(4-o-tolyl-pipe...

example 2a

Synthetic Route Towards 2-cyclopropyl-oxazole-4-carboxylic acid [4-methoxy-5-[3-(2-oxo-pyrrolidin-1-yl)-propylcarbamoyl]-2-(4-o-tolyl-piperazin-1-yl)-phenyl]-amide 2c

[0227]

[0228]Step 1: To a solution of 2-chloro-5-nitro-N-[3-(2-oxo-pyrrolidin-1-yl)-propyl]-4-(4-o-tolyl-piperazin-1-yl)-benzamide 1f (350.0 mg, 0.70 mmol) in methanol (10.0 ml) was added sodium methoxide (378.1 mg, 7.0 mmol) and the reaction was stirred at 45° C. for 6 h. The reactions mixture was concentrated, water was added carefully and extracted with ethyl acetate. Organic layer was washed with water and brine and concentrated. Crude 2a was purified on silica gel using dichloromethane / MeOH (10%) to give product (248 mg, 71%).

[0229]Step 2: 2-Methoxy-5-nitro-N-[3-(2-oxo-pyrrolidin-1-yl)-propyl]-4-(4-o-tolyl-piperazin-1-yl)-benzamide 2a (350.0 mg, 0.706 mmol) was taken in ethanol and evacuated and nitrogen purged. This was added to a flask containing Pd / C (5 wt %) (300.6 mg, 0.141 mmol) under nitrogen. Flask was evacu...

example 2b

Synthetic Route Towards 2-cyclopropyl-oxazole-4-carboxylic acid [4-hydroxy-5-[3-(2-oxo-pyrrolidin-1-yl)-propylcarbamoyl]-2-(4-o-tolyl-piperazin-1-yl)-phenyl]-amide 2d

[0233]

[0234]To a solution of 2-cyclopropyl-oxazole-4-carboxylic acid [4-methoxy-5-[3-(2-oxo-pyrrolidin-1-yl)-propylcarbamoyl]-2-(4-o-tolyl-piperazin-1-yl)-phenyl]-amide 2c (40.0 mg, 0.067 mmol) in pyridine (5.0 mL) was added magnesium bromide (49.0 mg, 0.268 mmol). The reaction was stirred at 130° C. for 16 h. Cooled, concentrated and the crude 2d was dissolved in methanol / water mixture and purified on preparative HPLC using methanol / water as eluent.

[0235]LCMS (ESI) 587 (M+H);

[0236]1H NMR (400 MHz, DICHLOROMETHANE-d2) δ ppm 1.14 (d, J=2.34 Hz, 4H) 1.70-1.85 (m, 2H) 2.00-2.14 (m, 3H) 2.34 (s, 3H) 2.42 (d, J=8.30 Hz, 2H) 3.04-3.19 (m, 8H) 3.31-3.45 (m, 4H) 6.76 (s, 1H) 6.92-7.04 (m, 1H) 7.18 (d, J=13.42 Hz, 3H) 7.85-7.99 (m, 1H) 8.10 (s, 1H) 8.70 (s, 1H) 9.41-9.60 (m, 1H) 12.83 (s, 1H).

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Abstract

Novel benzamide derivatives of formula (I)wherein W1, W2, R1 to R10 and X have the meaning according to the claims, are positive allosteric modulators of the FSH receptor, and can be employed, inter alia, for the treatment of fertility disorders.

Description

RELATED APPLICATIONS[0001]This application is a continuation of U.S. Ser. No. 14 / 364,193 filed Jun. 10, 2014, which is a National Stage application of PCT Application PCT / US13 / 20802, filed Jan. 9, 2013, which claims priority to U.S. Provisional Application Ser. No. 61 / 585,077, filed Jan. 10, 2012.FIELD OF THE INVENTION[0002]The present invention relates to compounds of formula (I)wherein W1, W2, R1 to R10 and X have the meaning according to the claims, and / or physiologically acceptable salts thereof. The compounds of formulas (I) can be used as positive allosteric modulators of the follicle stimulating hormone receptor (FSHR). Objects of the invention are also pharmaceutical compositions comprising the compounds of formula (I), and the use of the compounds of formula (I) for the treatment of fertility disorders.BACKGROUND[0003]Gonadotropins serve important functions in a variety of bodily functions including metabolism, temperature regulation and the reproductive process. Gonadotrop...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C07D413/12A61D19/02C07D263/34A61D19/04A61K31/496C07D405/12
CPCC07D413/12A61K31/496A61D19/02C07D263/34A61D19/04C07D405/12C07D307/68C07D413/14C07D405/14C07D407/12A61P15/08A61P43/00A61B17/435
Inventor YU, HENRYRICHARDSON, THOMAS E.BHARATHI, PANDIHEASLEY, BRIAN H.JENKS, MATTHEW G.FOGLESONG, ROBERT J.
Owner MERCK PATENT GMBH
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