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Energy Chemical
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marketing@energy-chemical.com |
| Products Intro: |
Product Name:Clometacin
CAS:25803-14-9
Purity:NULL Package:250mg;25mg Remarks:NULL
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CLEARSYNTH LABS LTD.
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+91-22-45045900 |
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sales@clearsynth.com |
| Products Intro: |
Product Name:Clometacin
CAS:25803-14-9
|
| Company Name: |
United States Biological
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800.520.3011 or 781.639.5092 |
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chemicals@usbio.net |
| Products Intro: |
Product Name:Clometacin
CAS:25803-14-9
|
| Company Name: |
Debye Scientific Corporation
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00852-2521 1836 |
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| Products Intro: |
Product Name:2-(3-(4-chlorobenzoyl)-6-methoxy-2-methyl-1H-indol-1-yl)acetic acid
CAS:25803-14-9
|
|
| | clometacin Basic information |
| Product Name: | clometacin | | Synonyms: | 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;clometacin;1H-Indole-1-acetic acid, 3-(4-chlorobenzoyl)-6-methoxy-2-methyl-;C 1656;C1656;C-1656 | | CAS: | 25803-14-9 | | MF: | C19H16ClNO4 | | MW: | 357.791 | | EINECS: | 2472713 | | Product Categories: | | | Mol File: | 25803-14-9.mol |  |
| | clometacin Chemical Properties |
| Melting point | 242° | | Boiling point | 564.0±50.0 °C(Predicted) | | density | 1.32±0.1 g/cm3(Predicted) | | pka | 4.04±0.10(Predicted) |
| | clometacin Usage And Synthesis |
| Originator | Clometacin,Roussel-Uclaf | | Uses | Clometacin is an antalgic drug that binds to human serum albumin (HSA) and inhibits the binding of indomethacin, warfarin, clofibrate and salicylic acid to HSA. | | Definition | ChEBI: Clometacin is a N-acylindole. | | 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 and
Preparation of 1-carboxymethyl-2-methyl-3-p-chlorobenzoyl-6-methoxy-indole
STEP A: 1-(2'-Nitro-4'-methoxyphenyl)-2-methyl-2-nitroethyl
ene
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 and
Step 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. |
| | clometacin Preparation Products And Raw materials |
|