셀레콕시브

셀레콕시브
셀레콕시브 구조식 이미지
카스 번호:
184007-95-2
한글명:
셀레콕시브
동의어(한글):
셀레콕시브
상품명:
CELECOXIB
동의어(영문):
Ccris 8679;Celecoxib [old rn]
CBNumber:
CB91267649
분자식:
포뮬러 무게:
0
MOL 파일:
184007-95-2.mol

셀레콕시브 속성

안전

셀레콕시브 C화학적 특성, 용도, 생산

Originator

Celact,Sun Pharmaceuticals Industries Ltd.,India

Manufacturing Process

4-(5-(4-Methylphenyl)-3-trifluoromethyl-N-pyrazol-1-yl)benzenesulfonamide To a solution of ethyl trifluoroacetate (1.90 ml, 16.0 mmol) in 7 ml of methyl tert-butyl ether was added 25% NaOMe (3.62 ml, 16.8 mmol). Next 4- chloroaceteophenone (2.08 ml, 16.0 mmol) in 2 ml of methyl tert-butyl ether was added. The mixture was stirred at room temperature overnight. To above solution was added 100 ml of 90% EtOH, followed by 4 N HCl (4.0 ml, 16 mmol) and 4-sulphonamidophenylhydrazine hydrochloride (3.58 g, 16 mmol). The mixture was heated to reflux for 3 hours. The mixture was concentrated. When 30 ml of water was added, a solid formed. The solid was filtered and washed with 20 ml of 60% EtOH to give 4.50 g of white solid. The filtrate was evaporated and taken up in ethyl acetate (100 ml), washed with saturated NaHCO3, and brine, dried over MgSO4, and concentrated. Heptane was added at boiling point of the mixture. After cooling down to 0°C, 1.01 g more product was obtained. The combined yield of the 4-(5-(4-methylphenyl)-3- trifluoromethyl-N-pyrazol-1-yl)benzenesulfonamide (Celecoxib) was 86%.

Therapeutic Function

Antiinflammatory

셀레콕시브 준비 용품 및 원자재

원자재

준비 용품


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