|
| | alminoprofen Basic information |
| Product Name: | alminoprofen | | Synonyms: | alminoprofen;ALMINOPROFEN(FORR&DONLY);EB 382;Minalfene;2-[4-(Methallylamino)phenyl]propanoic acid;4-[(2-Methyl-2-propenyl)amino]hydratropic acid;Minalfen;α-Methyl-4-[(2-methyl-2-propenyl)amino]benzeneacetic acid | | CAS: | 39718-89-3 | | MF: | C13H17NO2 | | MW: | 219.28 | | EINECS: | 254-604-6 | | Product Categories: | | | Mol File: | 39718-89-3.mol |  |
| | alminoprofen Chemical Properties |
| Melting point | 107° | | Boiling point | 360.1°C (rough estimate) | | density | 1.0697 (rough estimate) | | refractive index | 1.5100 (estimate) | | storage temp. | -20°C Freezer | | solubility | Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) | | pka | 4.86±0.50(Predicted) | | form | Solid | | color | Light Brown |
| Toxicity | LD50 orally in mice: 2400 mg/kg (Dumaitre) |
| | alminoprofen Usage And Synthesis |
| Description | Alminoprofen is an arylpropionic acid analgesic/antiinflammatory agent indicated
for the short term management of dental, traumatic and postpartum pain. | | Originator | Labs. Dr. E. Bouchara (France) | | Uses | Alminoprofen is a nonsteroidal antiinflammatory drugs (NSAID) of the phenylpropionic acid class. Alminoprofen maybe a useful therapeutic option in the management of immune dysfunction in rheumatoid ar
thritis. | | Definition | ChEBI: A substituted aniline that is ibuprofen in which the isobutyl group is replaced by a (2-methylprop-2-en-1-yl)amino group. A non-steroidal anti-inflammatory drug, it is used for treatment of inflammatory and rheumatic disorders. | | Manufacturing Process | Methyl 2-(p-aminophenyl)propionate:
Methyl 2-(p-nitrophenyl)acrylate (52 g) is hydrogenated in ethanol (500 ml) in
the presence of 5% palladium-over-charcoal, while maintaining the
temperature at +5°C. The theoretical amount of hydrogen is taken up within
one hour. After separation of the catalyst and concentration to dryness, the
resulting material gives methyl 2-(p-aminophenyl)proprionate which
crystallizes: MP: = 40°-43°C.
Methyl 2-(p-methallylaminophenyl)propionate hydrochloride:
A mixture of methyl 2-(p-aminophenyl)propionate (44.75 g), methallyl
chloride (34 g) and pyridine (30 ml) in isopropanol (400 ml) is boiled during
30 hours. The solvent is removed in vacuo and the residue is taken up into
water and ether. After separation, the organic phase is washed repeatedly
with water, after which it is dried and concentrated in vacuo. The resulting oil
is fractionally distilled in vacuo (0.1 mm Hg; 5 g of oil essentially consisting of
methyl 2-(p-aminophenyl)propionate are collected at 115°-120°C; 30 g of oil
consisting of a mixture of mono- (80%) and disubstituted (20%) amines is
collected at 128°-130°C. This oil is used to prepare the hydrochloride, which
is recrystallized from ethyl acetate, to give white crystals (22.7 g) melting at 115°C. Saponification in the cold methanolic hydroxide gives the desired 2-(4-
(methallylamino)phenyl)propionic acid (alminoprofen). MP: 120°C. | | Brand name | MINALFENE | | Therapeutic Function | Analgesic, Antiinflammatory |
| | alminoprofen Preparation Products And Raw materials |
|
