옥사플루마진

옥사플루마진
옥사플루마진 구조식 이미지
카스 번호:
16498-21-8
한글명:
옥사플루마진
동의어(한글):
옥사플루마진
상품명:
Oxaflumazine
동의어(영문):
SD 270-31;Oxaflumazine;Oxaflumazine D8;10-{3-[4-(2-[1,3]dioxan-2-yl-ethyl)-piperazin-1-yl]-propyl}-2-trifluoromethyl-10H-phenothiazine;10-[3-[4-[2-(1,3-Dioxan-2-yl)ethyl]-1-piperazinyl]propyl]-2-(trifluoromethyl)-10H-phenothiazine;10H-Phenothiazine, 10-[3-[4-[2-(1,3-dioxan-2-yl)ethyl]-1-piperazinyl]propyl]-2-(trifluoromethyl)-
CBNumber:
CB71179401
분자식:
C26H32F3N3O2S
포뮬러 무게:
507.61
MOL 파일:
16498-21-8.mol

옥사플루마진 속성

끓는 점
605.5±55.0 °C(Predicted)
밀도
1.235±0.06 g/cm3(Predicted)
산도 계수 (pKa)
7.65±0.10(Predicted)

안전

옥사플루마진 C화학적 특성, 용도, 생산

Originator

Oxaflumine, Diamant ,France,1970

Manufacturing Process

Preparation of N-(3-chloropropyl)-N'-[2-(1,3-dioxanyl)-ethyl]-piperazine: A solution of 30 g (0.15 mol) of N-[2-(1,3-dioxanyl)-ethyl]-piperazine and 11.8 g (0.075 mol) of 1-bromo-3-chloropropane in 150 ml of dry benzene was refluxed with stirring for 5 hours. After cooling, the N-[2-(1,3-dioxanyl)ethyl]-piperazinium bromide which had precipitated was filtered off, the filtrate was concentrated in vacuo and the residual oil was distilled. 14.1 g (68%yield) of N-(3-chloropropyl)-N'-[2-1,3-dioxanyl)-ethyl]-piperazine which occurred as a light yellow oil were obtained. Boiling point: 152°C to 155°C under 0.07 mm Hg (nD23 = 1.4940). The disuccinate prepared in acetone and recrystallized from acetone melts at 104°C to 105°C on a hot stage microscope.
The sodium derivative of the 2-trifluoromethylphenothiazine was prepared from 26.7 g (0.1 mol) of 2-trifluoromethylphenothiazine and 2.3 g (0.1 g atom) of sodium in 500 ml of liquid ammonia. After the reaction was completed, the ammonia was driven off and 500 ml of dry toluene were added. A solution of 25 g (0.09 mol) of N-(3-chloropropyl)-N'-[2-(1,3dioxanyl)-ethyl]-piperazine in 200 ml of toluene was added drop by drop to this solution which was then refluxed with stirring for 18 hours. After cooling, the precipitate which had formed was filtered and the filtrate was washed with water, dried and concentrated in vacuo. 33 g of brown oil, the N-3-(2trifluoromethyl-10-phenothiazinyl)-propyl-N'-2-[2-(1,3-dioxanyl)]-ethylpiperazine, were obtained.
A warm solution of 4.4 g of the base obtained in 100 ml of acetonitrile was added to a warm solution of succinic acid in 200 ml of acetonitrile. After standing for 15 hours at 0°C. the crystalline product was obtained, melting point 138°C.

Therapeutic Function

Neuroleptic, Antihistaminic, Spasmolytic

옥사플루마진 준비 용품 및 원자재

원자재

준비 용품


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