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Organic compounds

a technology of organic compounds and compounds, applied in the field of organic compounds, can solve the problems of obsessive-compulsive disorder and related disorders, difficult treatment, and serious affecting the ability of people to obtain an adequate and effective education

Pending Publication Date: 2022-09-22
INTRA CELLULAR THERAPIES INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The compounds in this patent are active at multiple receptors and transporters, including serotonin receptors, serotonin transporters, dopamine receptors, and Mu-opiate receptors. They also have the unique activity of a biased ligand at the Mu-opiate receptor. Additionally, it is believed that they may enhance the signaling of NMDA and AMPA through the mTOR pathway through their activity at the D1 receptor.

Problems solved by technology

Obsessive-compulsive disorder (OCD) and related disorders, have become highly prevalent and are difficult to treat.
Half of people who suffer from OCD begin to show symptoms before the age of 20, which can seriously affect their ability to obtain an adequate and effective education.
Without effective treatment, however, the disease can last for decades.
A significant number of patients either do not respond to these agents, or cannot handle the side effects caused by these agents.
However, strong opiate agents can be addictive, and their use may be contraindicated in some patients.
Drug dependency disorders, such as opiate use disorder (OUD), are another group of disorders which are difficult to successfully treat.
Each of these agents has had limited success, and long-term adherence to prescribed therapies for OUD remains low.
In addition, these treatments often exacerbate common co-morbidities associated with OUD, such as mood and anxiety disorders, which further increases the risk of remission.
Abrupt opioid abuse withdrawal (i.e., going “cold turkey”) is also associated with severe side effects, including dysphoria, depression and anxiety, and the common treatment agents do not address these problems, and may make them worse.

Method used

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  • Organic compounds
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Examples

Experimental program
Comparison scheme
Effect test

example 1

of 4-((6bR,10aS)-2-oxo-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxalin-8-yl)-1-(4-fluoro-phenyl)-butan-1-one

[0363]

[0364](6bR, 10aS)-2-oxo-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxaline-8-carboxylic acid ethyl ester (6.4 g, 21.2 mmol) is suspended in HBr acetic acid solution (64 mL, 33% w / w) at room temperature. The mixture is heated at 50° C. for 16 h. After cooling, and treatment with ethyl acetate (300 mL), the mixture is filtered. The filter cake is washed with ethyl acetate (300 mL), and then dried under vacuum. The obtained HBr salt is then suspended in methanol (200 mL), and cooled with dry ice in isopropanol. Under vigorous stirring, ammonia solution (10 mL, 7N in methanol) is added slowly to the suspension to adjust the pH of the mixture to 10. The obtained mixture is dried under vacuum without further purification to give crude (6bR, 10aS)-2-oxo-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quin...

example 2

of 4-((6bR,10aS)-2-oxo-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxalin-8-yl)-1-(4-fluoro-phenyl)-butan-1-ol

[0366]

[0367]4-((6bR,10aS)-2-oxo-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxalin-8-yl)-1-(4-fluoro-phenyl)-butan-1-one (50 mg, 0.127 mmol) is dissolved in methanol (5 mL). Under stirring, NaBH4 (31 mg, 0.82 mmol) is added in batches. After the completion of the addition, the mixture is stirred at room temperature for 30 min. Methanol is evaporated under reduced pressure. The residue is dissolved in dichloromethane (10 mL) and then extracted with water (2×0.5 mL). The combined organic phase is dried over K2CO3. After filtration, the filtrate is concentrated under reduced pressure and then further dried under vacuum to give 4-((6bR,10aS)-2-oxo-2,3,6b,9,10,10a-hexahydro-1H,7H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxalin-8-yl)-1-(4-fluoro-phenyl)-butan-1-ol as a pale yellow foamy solid (45 mg, yield 90%). 1H NMR (500 MHz, DMS...

example 3

of (6bR,10aS)-8-(3-(4-fluorophenoxy)propyl)-6b,7,8,9,10,10a-hexahydro-1H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxalin-2(3H)-one

[0368]

[0369]A mixture of (6bR,10aS)-6b,7,8,9,10,10a-hexahydro-1H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxalin-2(3H)-one (100 mg, 0.436 mmol), 1-(3-chloroproxy)-4-fluorobenzene (100 μL, 0.65 mmol) and KI (144 mg, 0.87 mmol) in DMF (2 mL) is degassed with argon for 3 minutes and DIPEA (150 μL, 0.87 mmol) is added. The resulting mixture is heated to 78° C. and stirred at this temperature for 2 h. The mixture is cooled to room temperature and then filtered. The filter cake is purified by silica gel column chromatography using a gradient of 0-100% ethyl acetate in a mixture of methanol / 7N NH3 in methanol (1:0.1 v / v) as an eluent to produce partially purified product, which is further purified with a semi-preparative HPLC system using a gradient of 0-60% acetonitrile in water containing 0.1% formic acid over 16 min to obtain the title product as a solid (50 mg, yi...

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Abstract

The invention relates to particular substituted heterocycle fused gamma-carbolines, their prodrugs, in free, solid, pharmaceutically acceptable salt and / or substantially pure form as described herein, pharmaceutical compositions thereof, and methods of use in the treatment of diseases involving the 5-HT2A receptor, the serotonin transporter (SERT), pathways involving the dopamine D1 and D2 receptor signaling system, and / or the μ-opioid receptor.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]This application claims priority to U.S. Provisional Application No. 62 / 537,287, filed on Jul. 26, 2017; 62 / 639,244 filed on Mar. 6, 2018; and 62 / 682,546, filed on Jun. 8, 2018; the contents of each of which are incorporated by reference in their entirety.FIELD OF THE INVENTION[0002]The invention relates to new methods and uses pertaining to particular substituted heterocycle fused gamma-carbolines, their prodrugs, in free, solid, pharmaceutically acceptable salt and / or substantially pure form as described herein, and pharmaceutical compositions thereof, such as methods of use in the treatment of diseases involving the 5-HT2A receptor, the serotonin transporter (SERT), pathways involving dopamine D1 and D2 receptor signaling systems, and / or the μ-opioid receptor, e.g., diseases or disorders such as anxiety, psychosis, schizophrenia, sleep disorders, sexual disorders, migraine, conditions associated with cephalic pain, social phobias, gast...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): A61K31/4985A61P25/36A61P23/00A61K9/00A61K9/16A61K31/137A61K31/485A61K45/06
CPCA61K31/4985A61P25/36A61P23/00A61K9/0019A61K9/1647A61K31/137A61K31/485A61K45/06A61K31/5383A61K31/55A61P25/00A61K2300/00
Inventor LI, PENGYAO, WEIDAVIS, ROBERTMATES, SHARONVANOVER, KIMBERLYSNYDER, GRETCHEN
Owner INTRA CELLULAR THERAPIES INC
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