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Tolmetin

CAS No.
26171-23-3
Chemical Name:
Tolmetin
Synonyms
C07149;olmetin;McN 2559;Tolmetin;Methyiin;Tolmetine;TOLMETINUM;pyrolyzate;Tolmetin Solution, 100ppm;1-Methyl-5-p-toluoylpyrrole-2-acetic acid
CBNumber:
CB2875183
Molecular Formula:
C15H15NO3
Molecular Weight:
257.28
MDL Number:
MFCD00599595
MOL File:
26171-23-3.mol
Last updated:2024-12-18 14:08:52

Tolmetin Properties

Melting point 156 °C
Boiling point 400.53°C (rough estimate)
Density 1.1391 (rough estimate)
refractive index 1.5200 (estimate)
storage temp. 2-8°C
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
pka pKa 3.5(H2O t undefined I undefined) (Uncertain)
color Off-White to Pale Yellow
Water Solubility 222 mg/L
FDA UNII D8K2JPN18B
ATC code M01AB03,M02AA21
NIST Chemistry Reference Tolmetin(26171-23-3)
EPA Substance Registry System 1H-Pyrrole-2-acetic acid, 1-methyl-5-(4-methylbenzoyl)- (26171-23-3)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H302-H335-H319
Precautionary statements  P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501
Hazardous Substances Data 26171-23-3(Hazardous Substances Data)

Tolmetin price More Price(19)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC M332943 1-Methyl-5-p-toluoylpyrrole-2-aceticAcid 26171-23-3 100mg $70 2021-12-16 Buy
AK Scientific J10499 Tolmetin 26171-23-3 5mg $39 2021-12-16 Buy
Matrix Scientific 074159 1-Methyl-5-p-toluoylpyrrole-2-acetic acid 95+% 26171-23-3 1g $278 2021-12-16 Buy
ChemScene CS-W008734 Tolmetin ≥98.0% 26171-23-3 25g $504 2021-12-16 Buy
Matrix Scientific 074159 1-Methyl-5-p-toluoylpyrrole-2-acetic acid 95+% 26171-23-3 10g $1000 2021-12-16 Buy
Product number Packaging Price Buy
M332943 100mg $70 Buy
J10499 5mg $39 Buy
074159 1g $278 Buy
CS-W008734 25g $504 Buy
074159 10g $1000 Buy

Tolmetin Chemical Properties,Uses,Production

Description

An antiinflammatory, analgesic, and antipyretic that is as efficacious as moderate doses of aspirin and better tolerated. Tolmetin produces a number of adverse effects including epigastric pain, dyspepsia, nausea, and vomiting. Tolmetin is approximately 99% plasma protein bound, yet does not interfere with concurrent treatment with oral hypoglycemics. Tolmetin has been found to be effective in the treatment of osteoarthritis and rheumatoid arthritis.

Originator

Tolectin,McNeil,US,1976

Uses

inhibits synthesis of prostaglandins and exhibits expressed analgesic, anti-inflammatory, and fever-reducing properties. It is used for relieving weak to moderate pain in rheumatoid arthritis and osteoarthritis.

Uses

Tolmetine is an NSAID.

Indications

Tolmetin (Tolectin) is indicated for the relief of osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, and moderate pain. It is ineffective in gouty arthritis for unknown reasons.Tolmetin can inhibit both COX-1 and COX-2 but has a moderate selectivity for COX-1. The most frequently reported side effects are GI disturbance and CNS reactions (e.g., headache, asthenia, and dizziness). These effects are less frequently observed than after aspirin or indomethacin use. Blood pressure elevation, edema, and weight gain or loss have been associated with tolmetin administration. Tolmetin metabolites in urine have been found to produce pseudoproteinuria in some laboratory tests.

Definition

ChEBI: A monocarboxylic acid that is (1-methylpyrrol-2-yl)acetic acid substituted at position 5 on the pyrrole ring by a 4-methylbenzoyl group. Used in the form of its sodium salt dihydrate as a nonselective nonsteroidal anti-inflammatory drug.

Manufacturing Process

5-(p-Toluoyl)-1-methylpyrrole-2-acetonitrile - To a cooled suspension of 26.6 g (0.2 mol) aluminum chloride in 80 ml dichloroethane is added dropwise 30.8 g (0.2 mol) p-toluoyl chloride. The resulting solution is added dropwise to a solution of 1-methylpyrrole-2-acetonitrile in 80 ml dichloroethane cooled externally with an ice bath. After the addition, the resulting solution is stirred at room temperature for 20 minutes and then refluxed for 3 minutes. The solution is poured into ice acidified with dilute hydrochloric acid. The organic and aqueous fractions are separated. The aqueous fraction is extracted once with chloroform.
The organic fractions are combined and washed successively with N,N_x0002_dimethyl-1,3-propanediamine, dilute hydrochloric acid, saturated sodium bicarbonate solution and saturated sodium chloride solution. The organic fraction is dried over anhydrous magnesium sulfate. The solvent is then evaporated off. Upon trituration of the residue with methanol, a solid crystallizes, 5-(p-toluoyl)-1-methylpyrrole-2-acetonitrile, which is removed by filtration and purified by recrystallization from benzene.
Additional product is isolated from the mother liquors which are combined, concentrated in vacuo and the resulting oily residue column chromatographed on neutral alumina using hexane, benzene and ether as successive solvents. The product is isolated by concentrating in vacuo the first few major compound-bearing fractions (10% ether in benzene). The solids are combined and recrystallized from methanol and then from benzene-hexane, melting point 102°C to 105°C.
5-(p-Toluoyl)-1-methylpyrrole-2-acetic acid - A solution of 3.67 g (0.015 mol) of 5-(p-toluoyl)-1-methylpyrrole-2-acetonitrile, 24 ml of 1 N sodium hydroxide and 50 ml of 95% ethanol is stirred and refluxed for 24 hours. The resulting solution is poured into ice acidified with dilute hydrochloric acid. A white solid precipitates which is extracted into ether. The ether phase is washed with a saturated solution of sodium chloride and dried over anhydrous magnesium sulfate. The solvent is evaporated and a white solid, 5-(p-toluoyl)- 1-methylpyrrole-2-acetic acid is obtained which is recrystallized twice from isopropanol, melting point 155°C to 157°C.

Therapeutic Function

Antiinflammatory

Biological Functions

Tolmetin (Tolectin) is an antiinflammatory, analgesic, and antipyretic agent that produces the usual gastric distress and ulceration observed with NSAIDs. However, tolmetin is better tolerated than aspirin and produces less tinnitus and vertigo. Tolmetin is a substitute for indomethacin in indomethacin-sensitive patients and is unique among such drugs in that it can be used to treat juvenile arthritis.

General Description

Tolmetin sodium (Tolectin), is an arylacetic acid derivativewith a pyrrole as the aryl group. This drug is well absorbed and has a relatively short plasma half-life (1 hour). It is recommendedfor use in the management of acute and chronicRA. Its efficacy is similar to aspirin and indomethacin, butwith less frequency of the adverse effects and tinnitus associatedwith aspirin. It does not potentiate coumarin-likedrugs nor alter the blood levels of sulfonylureas or insulin.However, tolmetin, and especially its closely related drug,zomepirac (i.e., with a p-chlorobenzoyl group and an additionalmethyl group on the pyrrole ring), can produce a rarebut fatal anaphylactic reaction because of irreversible bindingof their unstable acyl glucuronides. Zomepirac waswithdrawn from market because it is eliminated only via theester-type, acyl glucuronide. It is possible that tolmetin isless toxic in this regard because it undergoes additional hepaticbenzylic hydroxylation via its p-methyl group and isexcreted as its stable ether glucuronide.

Trade name

Artrocaptin (Estedi, Spain), Tolectin (Cilag, Belgium; Janssen-Cilag, Austria; McNeil, USA).

Mechanism of action

Tolmetin inhibits both isoforms of cyclooxygenase with some preference for COX-1 .

Pharmacology

Tolmetin is administered orally, rectally, or topically (600–1800 mg/d). The peak plasma concentrations are reached within 30 to 60 min. Tolmetin shows a high plasma protein binding of 99% and a biphasic plasma half-life of 1 to 2 and 5h, respectively.

Clinical Use

Tolmetin is a nonsteroidal anti-inflammatory drug used for the treatment of mild to moderate pain states in musculoskeletal, soft-tissue, and joint disorders like rheumatoid arthritis, osteoarthritis, and gout as well as juvenile rheumatoid arthritis.

Synthesis

Tolmetin, 1-methyl-5-n-tolylpyrrol-2-acetic acid (3.2.61) is synthesized from 1- methylindole, which is aminomethylated using formaldehyde and dimethylamine, forming 2-dimethylaminomethyl-1-methylindol (3.2.57). The product is methylated by methyl iodide, giving the corresponding quaternary salt (3.2.58). Reaction of the product with sodium cyanide gives 1-methylpyrrole-2-acetonitrile (3.2.59), which is acylated at the free |á-position of the pyrrole ring by 4-methylbenzoylchloride in the presence of aluminum chloride. The resulting 1-methyl-5-n-toluylpyrrol-2-acetonitrile (3.2.60) undergoes further alkaline hydrolysis, giving corresponding acid, tolmetin (3.2.61) [116¨C118].

Synthesis_26171-23-3

Tolmetin Preparation Products And Raw materials

Global( 128)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Weibang Biotechnology Co., Ltd
+8615531157085 abby@weibangbio.com China 8810 58
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Alchem Pharmtech,Inc.
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career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29811 58

View Lastest Price from Tolmetin manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Tolmetin  pictures 2024-12-18 Tolmetin
26171-23-3
US $10.00 / kg 1kg 99% 20ton Hebei Zhuanglai Chemical Trading Co.,Ltd
Tolmetin pictures 2024-10-24 Tolmetin
26171-23-3
US $10.00 / KG 1KG 99% 10 mt Hebei Weibang Biotechnology Co., Ltd
Tolmetin pictures 2024-04-22 Tolmetin
26171-23-3
US $50.00 / kg 1kg 99.10% 50000kg Ouhuang Engineering Materials (Hubei) Co., Ltd
  • Tolmetin  pictures
  • Tolmetin
    26171-23-3
  • US $10.00 / kg
  • 99%
  • Hebei Zhuanglai Chemical Trading Co.,Ltd
  • Tolmetin pictures
  • Tolmetin
    26171-23-3
  • US $10.00 / KG
  • 99%
  • Hebei Weibang Biotechnology Co., Ltd
  • Tolmetin pictures
  • Tolmetin
    26171-23-3
  • US $50.00 / kg
  • 99.10%
  • Ouhuang Engineering Materials (Hubei) Co., Ltd
1-Methyl-5-p-toluoylpyrrole-2-acetic acid 5-[(p-Tolyl)carbonyl]-1-methylpyrrole-2-acetic acid McN 2559 1-Methyl-5-(4-methylbenzoyl)-1H-pyrrole-2-acetic acid 1-Methyl-5-(p-toluoyl)-1H-pyrrole-2-acetic acid C07149 2-(1-Methyl-5-(4-Methylbenzoyl)-1H-pyrrol-2-yl)acetic acid 2-{1-Methyl-5-[(4-Methylphenyl)carbonyl]-1H-pyrrol-2-yl}acetic acid 1H-Pyrrole-2-acetic acid, 1-methyl-5-(4-methylbenzoyl)- Tolmetine TOLMETINUM 2-[1-Methyl-5-(4-methylbenzoyl)-pyrrol-2-yl]acetic acid Tolmetin Solution, 100ppm Tolmetin 2-[1-methyl-5-[(4-methylphenyl)-oxomethyl]-2-pyrrolyl]acetic acid Methyiin pyrolyzate olmetin 26171-23-3 Inhibitors API API intermediates