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N-substituted benzenesulfonyl phenothiazine compound and its preparation method and use

A technology of compound and alkyl, which is applied in the field of medicine, can solve the problems of insufficient physical and chemical properties of benzazepine compounds such as activity and side effects

Active Publication Date: 2017-05-17
天津天诚新药评价有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] As drugs for the treatment of the above-mentioned diseases, benzazepine compounds still have certain deficiencies in terms of activity, side effects and physicochemical properties.

Method used

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  • N-substituted benzenesulfonyl phenothiazine compound and its preparation method and use
  • N-substituted benzenesulfonyl phenothiazine compound and its preparation method and use
  • N-substituted benzenesulfonyl phenothiazine compound and its preparation method and use

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0057] Preparation of IV-1

[0058]

[0059] II-1 (100g, 502mmol) was placed in a 1000mL reaction flask, and CH was added 2 Cl 2 (500mL) stirred to make it dissolve, added triethylamine (76g, 750mmol), stirred under ice-water bath, added intermediate III-1 (121.9g, 550mmol) in batches, kept the temperature and stirred for 1h, TLC detection showed that the reaction was finished ( Developing agent ethyl acetate:petroleum ether=1:3).

[0060] The reaction solution was poured into 500ml of cold water, fully shaken to separate the layers, and the organic layer was separated and washed three times in succession. The organic layer was dried over anhydrous sodium sulfate and left overnight. After filtration, the solvent was evaporated to dryness under reduced pressure to obtain a light yellow solid. The resulting product was recrystallized from ethanol to obtain 173 g of a light yellow solid. The purity is 97.9% (HPLC normalization method), and the yield is 89.6%. ESI-MS ([...

Embodiment 2

[0062] Preparation of IV-2

[0063]

[0064] II-1 (20g, 100mmol) was placed in a 250mL reaction flask, and CHCl was added 3 (100mL) was stirred to dissolve, added pyridine (8.7g, 110mmol), stirred and dissolved at 50°C, added intermediate III-2 (23.3g, 105mmol) in batches, kept stirring at the temperature for 3h, TLC detection showed that the reaction was complete (Developer ethyl acetate:petroleum ether=1:3).

[0065] The reaction solution was poured into 100ml of cold water, fully shaken to separate the layers, and the organic layer was separated and washed three times in succession. The organic layer was dried over anhydrous sodium sulfate and allowed to stand overnight. After filtration, the solvent was evaporated to dryness under reduced pressure to obtain a light yellow solid crude product. The resulting crude product was purified by silica gel column chromatography to obtain 34.8 g of a pale yellow solid. The purity is 98.2% (HPLC normalization method), and the...

Embodiment 3

[0067] Preparation of IV-3

[0068]

[0069] Put II-2 (20g, 86mmol) in a 250mL reaction flask, add pyridine (60mL), stir to dissolve, stir under ice-water bath, add intermediate III-3 (20.3g, 86mmol) in batches, keep the temperature and stir for 4h , TLC detection showed that the reaction was complete (developing agent ethyl acetate:petroleum ether=1:3).

[0070] The reaction solution was poured into 300ml of cold water, stirred, and solids were precipitated. After filtering, the filter cake was washed with water and dried to obtain a yellow crude product. The crude product was recrystallized from ethanol to obtain 34.7 g of a light yellow solid. The purity is 98.4% (HPLC normalization method), and the yield is 93.3%. ESI-MS ([M+H]+): 433.0.

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Abstract

The invention relates to N-substituted benzenesulfonyl phenothiazine compounds as well as a preparation method and application thereof, and particularly relates to N-substituted benzenesulfonyl phenothiazine compounds having a structure shown in a formula I described in the specification as well as a preparation method thereof, pharmaceutical compositions taking the N-substituted benzenesulfonyl phenothiazine compounds with a structure as shown in the formula I as active ingredients and use of the pharmaceutical compositions for preventing or treating diseases associated with an arginine vasopressin V1a receptor, an arginine vasopressin V1b receptor, an arginine vasopressin V2 receptor, a sympathetic nervous system or a rennin-angiotensin-aldosterone system.

Description

technical field [0001] The invention belongs to the technical field of medicine, more specifically, relates to a class of N-substituted benzenesulfonyl phenothiazine compounds and their preparation method and application. Background technique [0002] Arginine vasopressin (AVP), also known as antidiuretic hormone and vasopressin, is a peptide hormone secreted by the pituitary gland. It regulates body fluids through the receptor-G protein-second messenger pathway. Balance and other functions. AVP plays an important role in regulating the reabsorption of free water in the human body, the isotonic concentration of body fluids, blood volume, blood pressure, cell contraction, cell proliferation, and secretion of adrenal cortex hormones. [0003] Arginine vasopressin exerts various physiological effects by binding to vasopressin receptors. Vasopressin receptors can be divided into three subtypes, V1a, V1b and V2. V1a receptors are distributed in vascular smooth muscle, muscle c...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07D279/34A61K31/5415A61K31/635A61P9/12A61P15/00A61P5/38A61P9/04A61P1/16A61P5/00A61P3/14A61P25/24A61P25/14
CPCC07D279/32
Inventor 刘颖刘登科穆帅岳南龚珉支爽刘昌孝
Owner 天津天诚新药评价有限公司
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