25803-14-9

Basic information

• Product Name: clometacin
• Synonyms: clometacin;3-(4-Chlorobenzoyl)-6-methoxy-2-methylindole-1- acetic acid;C017136;2-(3-(4-chlorobenzoyl)-6-methoxy-2-methyl-1H-indol-1-yl)acetic acid
• CAS NO: 25803-14-9
• Molecular Formula: C₁₉H₁₆ClNO₄
• Molecular Weight: 357.791
• EINECS: 247-271-3
• Mol File: 25803-14-9.mol
• Article Data: 2

Chemical Properties

• Melting Point: 242°
• Boiling Point: 564°C at 760 mmHg
• Flash Point: 294.9°C
• Appearance: /
• Density: 1.32g/cm³
• Vapor Pressure: 1.47E-13mmHg at 25°C
• Refractive Index: 1.619
• PKA: 4.04±0.10(Predicted)
• CAS DataBase Reference: clometacin(CAS DataBase Reference)
• NIST Chemistry Reference: clometacin(25803-14-9)
• EPA Substance Registry System: clometacin(25803-14-9)

Safety Data

• Hazardous Substances Data: 25803-14-9(Hazardous Substances Data)

Usage

Description

Clometacin is an antalgic drug that possesses the ability to bind with human serum albumin (HSA) and interfere with the binding of other drugs such as indomethacin, warfarin, clofibrate, and salicylic acid to HSA. This interaction with HSA allows clometacin to serve as a potential candidate for various applications in the pharmaceutical industry.

Uses

Used in Pharmaceutical Applications:
Clometacin is used as an antalgic agent for the management of pain. Its ability to bind with human serum albumin (HSA) allows it to inhibit the binding of other drugs like indomethacin, warfarin, clofibrate, and salicylic acid to HSA, which can be beneficial in certain therapeutic situations where the interaction of these drugs with HSA needs to be controlled or minimized.
Additionally, clometacin's interaction with HSA can be utilized in the development of drug delivery systems, where it can be employed as a carrier or modulator to enhance the bioavailability and therapeutic outcomes of other drugs that share similar binding sites on HSA. This application can be particularly useful in the design of personalized medicine approaches, where the drug-HSA interaction can be tailored to individual patient needs.

Originator

Clometacin,Roussel-Uclaf

Manufacturing Process

Preparation of 1-carboxymethyl-2-methyl-3-p-chlorobenzoyl-6-methoxy-indole STEP A: 1-(2'-Nitro-4'-methoxyphenyl)-2-methyl-2-nitroethylene 15.0 g of 2-nitro-4-methoxybenzaldehyde (Boon, Soc., 1949 Suppl., p. 230) were introduced into a mixture of 75 ml of acetic acid, 9.5 ml of nitroethane and 6.5 gm of ammonium acetate and the resulting mixture was heated to reflux and held there for 2 h. After cooling the mixture to room temperature, the mixture was added to ice water and the precipitate formed was recovered by vacuum filtration. The precipitate was washed with water and twice crystallized from ethanol and treated with carbon black to obtain 9.6 gm of 1- (2'-nitro-4'-methoxyphenyl)-2-methyl-2-nitroethylene having a melting point of 111°C. STEP B: 2-Methyl-6-rnethoxyindole 32 g of 1-(2'-nitro-4'-methoxyphenyl)-2-methyl-2-nitroethylene and 3.2 g of palladized charcoal con training 18% palladium were introduced into a mixture of 320 ml of ethyl acetate, 48 ml of ethanol and 240 ml of acetic acid and after a purge with nitrogen then with hydrogen, the mixture was agitated under a hydrogen atmosphere. The reaction temperature was allowed to rise to 50°C and was held at that temperature by cooling. 18.2 L of hydrogen were absorbed in 3 h after which the reaction mixture was purged with nitrogen and the catalyst was removed by filtration. The reaction mixture was concentrated to dryness under reduced pressure and the residue was dissolved in methylene chloride. The methylene chloride solution was washed with an aqueous solution of sodium bicarbonate, with water, was dried and concentrated to dryness under reduced pressure. The residue was crystallized from petroleum ether (boiling point 65-75°C) and the resulting product was dissolved in ether. The ether solution was filtered over alumina and 6.4 g of 2- methyl-6-methoxy-indole having a melting point of 104°C were obtained there from. STEP C: 2-Methyl-3-p-chlorobenzoyl-6-methoxyindole 9 g of 2-methyl-6-methoxy-indole were added to a suspension of 20.6 g of N, N-dimethyl-p-chlorobenzamide and 6.4 ml of phosphorus oxychloride. The interior reaction temperature obtained was brought to 60°C and rapidly rose to 115°C, the temperature was reduced and held for 2 h at 85°C. The temperature was then reduced to 50°C and the reaction mixture was added to water and then 400 ml of ethanol were added thereto. The reaction mixture was adjusted to a pH of 10 by the addition of sodium hydroxide solution andPreparation of 1-carboxymethyl-2-methyl-3-p-chlorobenzoyl-6-methoxy-indole STEP A: 1-(2'-Nitro-4'-methoxyphenyl)-2-methyl-2-nitroethylene 15.0 g of 2-nitro-4-methoxybenzaldehyde (Boon, Soc., 1949 Suppl., p. 230) were introduced into a mixture of 75 ml of acetic acid, 9.5 ml of nitroethane and 6.5 gm of ammonium acetate and the resulting mixture was heated to reflux and held there for 2 h. After cooling the mixture to room temperature, the mixture was added to ice water and the precipitate formed was recovered by vacuum filtration. The precipitate was washed with water and twice crystallized from ethanol and treated with carbon black to obtain 9.6 gm of 1- (2'-nitro-4'-methoxyphenyl)-2-methyl-2-nitroethylene having a melting point of 111°C. STEP B: 2-Methyl-6-rnethoxyindole 32 g of 1-(2'-nitro-4'-methoxyphenyl)-2-methyl-2-nitroethylene and 3.2 g of palladized charcoal con training 18% palladium were introduced into a mixture of 320 ml of ethyl acetate, 48 ml of ethanol and 240 ml of acetic acid and after a purge with nitrogen then with hydrogen, the mixture was agitated under a hydrogen atmosphere. The reaction temperature was allowed to rise to 50°C and was held at that temperature by cooling. 18.2 L of hydrogen were absorbed in 3 h after which the reaction mixture was purged with nitrogen and the catalyst was removed by filtration. The reaction mixture was concentrated to dryness under reduced pressure and the residue was dissolved in methylene chloride. The methylene chloride solution was washed with an aqueous solution of sodium bicarbonate, with water, was dried and concentrated to dryness under reduced pressure. The residue was crystallized from petroleum ether (boiling point 65-75°C) and the resulting product was dissolved in ether. The ether solution was filtered over alumina and 6.4 g of 2- methyl-6-methoxy-indole having a melting point of 104°C were obtained there from. STEP C: 2-Methyl-3-p-chlorobenzoyl-6-methoxyindole 9 g of 2-methyl-6-methoxy-indole were added to a suspension of 20.6 g of N, N-dimethyl-p-chlorobenzamide and 6.4 ml of phosphorus oxychloride. The interior reaction temperature obtained was brought to 60°C and rapidly rose to 115°C, the temperature was reduced and held for 2 h at 85°C. The temperature was then reduced to 50°C and the reaction mixture was added to water and then 400 ml of ethanol were added thereto. The reaction mixture was adjusted to a pH of 10 by the addition of sodium hydroxide solution andStep D: Methyl ester of 1-carboxymethyl-2-methyl-3-p-chlorobenzoyl-6- methoxyindole前期 20 ml of dimethylformamide were added to 0.32 g of a 50% suspension of sodium hydride in oil and then a solution of 2 g of 2-methyl-3-pchlorobenzoyl-6-methoxy-indole in 20 ml of dimethylformamide was added thereto. After hydrogen evolution ceased, a solution of 1 g of methyl monochloroacetate in 5 ml of dimethylformamide was added and the reaction mixture was stirred overnight at room temperature. The mixture was evaporated to dryness and the residue was taken up in water and vacuum filtered. The crystals were washed with water and dried in vacuum at 60°C to obtain 2.5 g of product which was purified by recrystallization from hot and cold methanol to give 1.9 g of the methyl ester of 1-carboxymethyl-2-methyl- 3-p-chloro-benzoyl-6-methoxy-indole having a melting point of 148-149°C as yellow crystals. STEP E: 1-Carboxymethyl-2-methyl-3-p-chlorobenzoyl-6-methoxy-indole 2.25 g of potassium hydroxide were dissolved in 100 ml of methanol and 5 ml of water and then 7.45 g of the methylester of 1-carboxymethyl-2- methylchlorobenzoyl-6-methoxy-indole were added thereto. The mixture was heated at reflux for 1 h and then was concentrated to dryness. The residue was taken up in 70 ml of boiling water and the solution was filtered while hot. The filtrate was cooled to 20°C and acidified to a pH of 1 by the addition of 30 ml of 2 N hydrochloric acid. The precipitate was recovered by vacuum filtration and was washed with water, then methanol and finally ether and was dried at 70°C. The resulting 6.3 g of product was purified by recrystallization from ethanol to obtain 3.7 g of 1-carboxymethyl-2-methyl-3-p-chloro-benzoyl- 6-methoxyindole having a melting point of 242°C.

Therapeutic Function

Analgesic, Antiinflammatory

World Health Organization (WHO)

Clometacin, an analogue of indometacin, was introduced on the market in 1971. Subsequently several cases of severe - in some cases fatal - hepatitis were reported, which led in 1987 to the withdrawal of a high-dosage tablet formulation, while the indications for a lower dosage tablet were restricted and duration of the treatment was limited. Eventually all tablet formulations were removed from the market. Clometacin is not widely registered in other countries.

InChI:InChI=1/C19H16ClNO4/c1-11-18(19(24)12-3-5-13(20)6-4-12)15-8-7-14(25-2)9-16(15)21(11)10-17(22)23/h3-9H,10H2,1-2H3,(H,22,23)

Relevant articles and documents

In pursuit of non narcotic analgetic and antiinflammatory agents. 1 carboxyalkyl 3 acylindoles

The synthesis and study of different carboxyalcoyl 1 acyl 3 indoles has led to molecules endowed with analgesic properties associated with an anti inflammatory action of variable importance. In particular carboxymethyl 1 p chlorobenzoyl 3 methoxy 6 indole (RU 3959) has a strong analgesic activity and a remarkable tolerance which have been confirmed in clinical trials.