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Substituted Isoindoles

a technology of substituted isoindoles and isoindoles, which is applied in the field of substituted isoindoles, can solve the problems of high prevalence of alzheimer's disease in this population, disease becomes a greater and greater problem,

Inactive Publication Date: 2011-12-29
ASTRAZENECA AB
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The likelihood of developing Alzheimer's disease increases with age, and as the aging population of the developed world increases, this disease becomes a greater and greater problem.
This is thought to be due to the extra copy of the APP gene found in these patients, which leads to overexpression of APP and therefore to increased levels of Aβ causing the high prevalence of Alzheimer's disease seen in this population.

Method used

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  • Substituted Isoindoles
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Examples

Experimental program
Comparison scheme
Effect test

example 1i

5-Bromo-2-fluoro-benzoyl chloride

[0228]

[0229]To a suspension of 5-bromo-2-fluoro-benzoic acid (10.0 g, 45.7 mmol) in anhydrous dichloromethane (200 mL) was added oxalyl chloride (5.2 mL, 59.4 mmol) followed by addition of anhydrous DMF (0.2 mL). The reaction mixture was stirred at room temperature overnight, then concentrated to dryness in vacuo to give title compound in quantitative yield, which was used directly in the next step.

[0230]1H NMR (400 MHz, CDCl3) δ ppm 8.22 (dd, 1H), 7.77-7.73 (m, 1H), 714 (dd, 1H); 19F NMR (400 MHz, CDCl3) δ ppm −110.55

example 2i

2-Methoxy-isonicotinoyl chloride

[0231]

[0232]Thionyl chloride (30.0 mL, 0.39 mol) was added to a suspension of 2-methoxy-isonicotinic acid (15.0 g, 97.9 mmol) in anhydrous toluene (150 mL). The mixture was heated at 80° C. under nitrogen for 3 hours, cooled to room temperature and filtered. The filtrate was concentrated in vacuo to afford the title compound 7.7 g (46% yield).

[0233]1H NMR (400 MHz, CDCl3) δ ppm 8.36 (d, 1H), 5.30 (d, 1H), 7.38 (s, 1H), 4.00 (s, 3H).

example 3i

2-(3-Bromobenzoyl)-6-fluorobenzonitrile

[0234]

[0235]A solution of copper(I) cyanide (4.70 g, 52.50 mmol) and lithium bromide (2.63 mL, 105.00 mmol) in THF (65 mL) was added to (2-cyano-3-fluorophenyl)zinc(II) iodide (100 mL, 50 mmol) at −78° C. under an argon atmosphere. The mixture was stirred at r.t. for 1 h and then cooled to −78° C. 3-Bromobenzoyl chloride (6.94 mL, 52.50 mmol) was added dropwise and the mixture was stirred at r.t. for 4 h. NH4Cl (50 mL, sat aq) was added followed by water (50 mL). The THF was removed in vacuo and the aqueous residue was diluted with water (100 mL) and DCM (150 mL). A precipitate was filtered off and the filtrate was added to a separation funnel. The organic layer was separated and the water phase extracted with DCM (100 mL). The combined organics were washed with brine (150 mL), dried over MgSO4, concentrated and purified on a silica gel column eluted with DCM to give the title compound (13.37 g, 88% yield): MS (ES+) m / z 304, 306 [M+H]+.

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Abstract

The present invention relates to novel compounds of formula (I) and their pharmaceutical compositions. In addition, the present invention relates to therapeutic methods for the treatment and / or prevention of Aβ-related pathologies such as Downs syndrome, β-amyloid angiopathy such as but not limited to cerebral amyloid angiopathy or hereditary cerebral hemorrhage, disorders associated with cognitive impairment such as but not limited to MCI (“mild cognitive impairment”), Alzheimer Disease, memory loss, attention deficit symptoms associated with Alzheimer disease, neurodegeneration associated with diseases such as Alzheimer disease or dementia including dementia of mixed vascular and degenerative origin, pre-senile dementia, senile dementia and dementia associated with Parkinson's disease, progressive supranuclear palsy or cortical basal degeneration.

Description

TECHNICAL FIELD OF THE INVENTION[0001]The present invention relates to novel compounds and their pharmaceutical compositions. In addition, the present invention relates to therapeutic methods for the treatment and / or prevention of Aβ-related pathologies such as Downs syndrome, β-amyloid angiopathy such as but not limited to cerebral amyloid angiopathy or hereditary cerebral hemorrhage, disorders associated with cognitive impairment such as but not limited to MCI (“mild cognitive impairment”), Alzheimer Disease, memory loss, attention deficit symptoms associated with Alzheimer disease, neurodegeneration associated with diseases such as Alzheimer disease or dementia including dementia of mixed vascular and degenerative origin, pre-senile dementia, senile dementia and dementia associated with Parkinson's disease, progressive supranuclear palsy or cortical basal degeneration.BACKGROUND[0002]Several groups have identified and isolated aspartate proteinases that have β-secretase activity ...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/4439C07D401/04A61P25/28A61K31/444A61K31/497A61P25/00C07D401/14A61K31/506
CPCC07D401/04C07D403/10C07D403/04C07D401/14A61P25/00A61P25/28A61P43/00A61P9/00A61K31/506
Inventor HOLENZ, JORGKARLSTROM, SOFIAKOLMODIN, KARINLINDSTROM, JOHANRAKOS, LASZLOROTTICCI, DIDIERSODERMAN, PETERSWAHN, BRITT-MARIEVON BERG, STEFAN
Owner ASTRAZENECA AB
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