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SUBSTITUTED IMIDAZO[1,5-a]PYRAZINES AS CGRP RECEPTOR ANTAGONISTS

a technology of imidazo[1,5-a]pyrazines and cgrp receptors, applied in the field of compounds, can solve the problems of lack of molecular evidence and cgrp2 receptor

Inactive Publication Date: 2018-02-01
BRISTOL MYERS SQUIBB CO
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The invention is about a series of compounds that can be used to treat various medical conditions. These compounds are designed to target a protein called CGRP, which is involved in the regulation of blood flow and inflammation. The compounds are antagonists of CGRP, meaning they are designed to prevent CGRP from causing certain effects. The invention includes various forms of these compounds, such as salts and prodrugs, and methods for making them. The technical effect of the invention is the development of new compounds that can be used to treat medical conditions related to CGRP, such as migraines and inflammatory diseases.

Problems solved by technology

However, there is lack of molecular evidence for the CGRP2 receptor (Brain, S. D. et al, TiPS 2002, 23, 51-53).

Method used

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  • SUBSTITUTED IMIDAZO[1,5-a]PYRAZINES AS CGRP RECEPTOR ANTAGONISTS
  • SUBSTITUTED IMIDAZO[1,5-a]PYRAZINES AS CGRP RECEPTOR ANTAGONISTS
  • SUBSTITUTED IMIDAZO[1,5-a]PYRAZINES AS CGRP RECEPTOR ANTAGONISTS

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0085]

[0086](±)-1-(7-Benzyl-5,6,7,8-tetrahydroimidazo [1,5-a]pyrazin-3-yl)-2-7-methyl-1H-indazol-5-yl)ethyl 4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxylate. (±)-1-(7-benzyl-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazin-3-yl)-2-(7-methyl-2-((2-(trimethylsilyDethoxy)methyl)-2H-indazol-5-yl)ethyl 4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxylate (365 mg, 0.47 mmol) was dissolved in trifluoroacetic acid (50% in dichloromethane, 10 mL) at room temperature. After 2.5 h, the reaction was concentrated. The reaction was purified by column chromatography (5% McOH / DCM→7.5% MeOH / DCM). The residue was re-purified by preparative HPLC. The resulting residue was passed through a shorty column of basic alumina (eluting with 10% McOH / DCM to give 120 mg (40%) as a white foam solid. LC / MS (Analytical HPLC method 1): tr=2.79 min; Mass spec.: 642.35 (MH)+.

example 2 and example 3

[0087]

[0088](1)-1-(7-Ethyl-5,6,7,8-tetrahydroinidazo[1,5-a]pyrazin-3-yl)-2-(7-methyl-1H-indazol-5-yl)ethyl 4-(2-oxo-1,2-dihydroquinoin-3-yl)piperidine-1-carboxylate and 2-(7-methyl-1H-indazol-5-yl)-1-(5,6,7,8-tetranydronnidazo[1,5-a]pyrazin-3-yl)ethyl 4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxylate. A suspension of (±)-1-(7-benzyl-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazin-3-yl)-2-(7-methyl-1H-indazol-5-yl)ethyl 4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxylate (75 mg, 0.12 mmol), palladium (10% on charcoal, 25 mg), and ammonium formate (74 mg, 1.2 mmol) in ethanol (3 mL) was heated at reflud for 2 h, occasionally knocking the sublimed ammonium formate back into the reaction with a spatula. The reaction was cooled, diluted with dichloromethane, filtered, and concentrated. Column chromatography (5% MeOH / DCM→20% MeOH / DCM) gave two fractions. The first to elute was (±)-1-(7-ethyl-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazin-3-yl)-2-(7-methyl-1H-indazol-5-yl)ethyl 4-(2-oxo-1...

example 4

[0089]

[0090](±)-1-(7-Cyclohexyl-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazin-3-yl)-2-(7-methyl-1H-indazol-5-yl)ethyl 4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxylate. To a solution of (±)-2-(7-methyl-1H-indazol-5-yl)-1-(5,6,7,8-tetrahydroimidazo[1,5-a]pyrazin-3-yl)ethyl 4-(2-oxo-1,2-dihydroquinolin-3-yl)piperidine-1-carboxylate (15 mg, 0.027 mmol) and cyclohexanone (5.7 μL, 0.054 mmol) in ethanol (1 mL) at room temperature was added sodium cyanoborohydride (3.4 mg, 0.054 mmol). After 5 min, one small drop of acetic acid was added. The reaction was treated with a second portion of cyclohexanone (5.7 μL, 0.054 mmol), followed by a second portion of sodium cyanoborohydride (3.4 mg, 0.054 mmol). After 30 min, the reaction was concentrated and purified by column chromatography (5% →10% MeOH / DCM) gave 11.3 mg (66%) as a white powder. LC / MS (Analytical HPLC method 2): tr=1.99 min; Mass spec.: 634.36 (MH)+.

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Abstract

The disclosure generally relates to the novel compounds of formula I, including pharmaceutically acceptable salts, which arc CGRP-receptor antagonists. The disclosure also relates to pharmaceutical compositions and methods for using the compounds in the treatment of CGRP related disorders including migraine headaches, neurogenic vasodilation, neurogenic inflammation, thermal injury, circulatory shock, flushing associated with menopause, airway inflammatory diseases such as asthma, and chronic obstructive pulmonary disease (COPD).

Description

BACKGROUND OF THE INVENTION[0001]The disclosure generally relates to the novel compounds of formula I, including pharmaceutically acceptable salts, which are CGRP-receptor antagonists. The disclosure also relates to pharmaceutical compositions and methods for using the compounds in the treatment of CGRP related disorders including migraine headaches, neurogenic vasodilation, neurogenic inflammation, thermal injury, circulatory shock, flushing associated with menopause, airway inflammatory diseases such as asthma, and chronic obstructive pulmonary disease (COPD).[0002]Calcitonin gene-related peptide (CGRP) is a naturally occurring 37-amino-acid peptide first identified in 1982 (Amara, S. G. et al, Science 1982, 298, 240-244). Two forms of the peptide are expressed (αCGRP and βCGRP) which differ by one and three amino acids in rats and humans, respectively. The peptide is widely distributed in both the peripheral (PNS) and central nervous system (CNS), principally localized in sensory...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C07D487/04
CPCC07D487/04A61P11/06A61P25/06
Inventor DEGNAN, ANDREW P.
Owner BRISTOL MYERS SQUIBB CO
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