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ChemicalBook--->CAS DataBase List--->34552-84-6

34552-84-6

34552-84-6 Structure

34552-84-6 Structure
IdentificationBack Directory
[Name]

ISOXICAM
[CAS]

34552-84-6
[Synonyms]

Pacyl
W 8495
Vectren
Maxicam
ISOXICAM
Isoxicamo
Isoxicamum
)-,1,1-dioxide
pacyl(antiinflammatory)
2h-1,2-benzothiazine-3-carboxamide,4-hydroxy-2-methyl-n-(5-methyl-3-isoxazolyl
4-Hydroxy-2-methyl-N-(5-methyl-3-isoxazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide
2H-1,2-Benzothiazine-3-carboxamide, 4-hydroxy-2-methyl-N-(5-methyl-3-isoxazolyl)-, 1,1-dioxide
[EINECS(EC#)]

252-084-5
[Molecular Formula]

C14H13N3O5S
[MDL Number]

MFCD00079374
[MOL File]

34552-84-6.mol
[Molecular Weight]

335.34
Chemical PropertiesBack Directory
[Melting point ]

265-271℃
[density ]

1.588
[storage temp. ]

-20°C Freezer
[solubility ]

Chloroform (Slightly, Heated), DMSO (Slightly), Methanol (Slightly, Heated, Sonicated)
[form ]

neat
[pka]

4.50±1.00(Predicted)
[color ]

White to Pale Beige
Safety DataBack Directory
[WGK Germany ]

2
[RTECS ]

DL0703000
[Toxicity]

LD50 in rats (mg/kg): >5000 orally (Whitehouse)
Hazard InformationBack Directory
[Description]

Isoxicam is a non-steroidal antiinflammatory agent useful in the treatment of various forms of rheumatoid arthritis, osteoarthritis and musculoskeletal disorders. It is about one-tenth as potent as its structural relative sudoxicam; its similar long T1/2 (>30 hrs.) allows once-daily dosing.
[Originator]

Warner-Lambert (USA)
[Uses]

antiseborrheic
[Uses]

Isoxicam is used for the same indications as piroxicam. Synonyms for isoxicam are floxicam and maxicam.
[Definition]

ChEBI: A monocarboxylic acid amide that is piroxicam in which the pyrid-2-yl group is replaced by a 5-methyl-1,2-oxazol-3-yl group. A non-steroidal anti-inflammatory drug, it was withdrawn from the market in the 1980s following its association with cases of Steve s-Johnson syndrome.
[Manufacturing Process]

A mixture of 40.5 g (0.15 mol) of 3-carbethoxy-4-hydroxy-2-methyl-2H-1,2- benzothiazine 1,1-dioxide, 20.6 g (0.21 mol) of 3-amino-5-methylisoxazole, and 2,500 ml of xylene was refluxed for 24 hours in a Soxhlet apparatus, the thimble of which contained 60 g of Linde type 4A molecular sieve. The mixture was cooled to 25°C and the resulting crystalline precipitate was collected and washed with ether to give 44 g of crude product. Recrystallization from 1,600 ml of 1,4-dioxan gave 34.7 g of material, MP 265°C to 271°C dec.
[Brand name]

Maxicam (Parke-Davis);Floxicam;PACYL.
[Therapeutic Function]

Antiinflammatory
[World Health Organization (WHO)]

Isoxicam, a nonsteroidal anti-inflammatory agent, was introduced in 1983 for the treatment of rheumatic disorders. By 1985 its use had been associated with serious adverse effects, including four deaths from rare skin reactions. This led to its withdrawal in France followed immediately by the voluntary suspension of marketing worldwide by the major manufacturer.
[Clinical Use]

Isoxicam is a nonsteroidal anti-inflammatory drug withdrawn from the market as a consequence of reports of fatal skin reaction.
[Synthesis]

Isoxicam, 1,1-dioxide 4-hydroxy-2-methyl-N-(5-methyl-3-isoxazolyl)-2H-1,2- benzothiazine-3-carboxamide (3.2.80), is synthesized analogous to piroxicam, using amidation of 1,1-dioxide 3-methoxycarbonyl-3,4-dihydro-2-H-1,2-benzothiazine-4-one (3.2.78) in the last stage with 3-amino-5-methylisoxazole, instead of 2-aminopyridine [127¨C130].

Synthesis_34552-84-6

Spectrum DetailBack Directory
[Spectrum Detail]

ISOXICAM(34552-84-6)1HNMR
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