BAMIPINE

BAMIPINE 구조식 이미지
카스 번호:
4945-47-5
상품명:
BAMIPINE
동의어(영문):
Soventol;BAMIPINE;Taumidrin;Piperamine;BAMIPINE USP/EP/BP;4-(N-Benzylanilino)-1-methylpiperidine;N-benzyl-N-(1-methyl-4-piperidyl)aniline;N-Benzyl-1-methyl-N-phenyl-4-piperidinamine;4-(N-Benzyl-N-phenylamino)-1-methylpiperidine;4-(n-benzyl-n-phenylamino)-1-methyl-piperidin
CBNumber:
CB3372285
분자식:
C19H24N2
포뮬러 무게:
280.41
MOL 파일:
4945-47-5.mol

BAMIPINE 속성

녹는점
115°
끓는 점
413.12°C (rough estimate)
밀도
0.9608 (rough estimate)
굴절률
1.8676 (estimate)
산도 계수 (pKa)
pKa 3.34±0.04 (H2O t unde?ned I=0.30(NaCl)) (Uncertain);8.04±0.11(H2O t unde?ned I=0.30(NaCl)) (Uncertain)

안전

BAMIPINE C화학적 특성, 용도, 생산

Originator

Bamipine,Pharm Chemical

Manufacturing Process

80 g of 1-methyl-piperidone-4 and 70 g of aniline are boiled, using a water separator in 350 ml of toluene to which several drops of glacial acetic acid have been added, until the theoretical quantity of water (12.7 ml) has separated out. The toluene is then distilled off and the remains are fractionated at reduced pressure. At a boiling point of 156°C/13 mm of Hg pressure, 118 g of a weakly yellow colored oil of the anil of 1-methyl-1- piperidone-4 are obtained.
100 g of the above described anil of 1-methyl-1-piperidone-4 are boiled for 8 hours, using a reflux condenser, with 30 g of activated borings of aluminum in 300 ml of methanol diluted with 60 ml of water. The liquid phase is then separated from the solid phase, the solvent is evaporated and the residuum is fractionated at reduced pressure, 95 g of a colorless oil being obtained boiling at 163-165°C at 15 mm of Hg pressure. The oil solidifies at once to a mass of crystals of 4-N-phenylaimno-1-methylpiperidine. After having been recrystallized from dibutyl ether the base melts at 87°C, its dihydrochloride has the melting point of 246°C.
95 g of 4-N-phenylamino-1-methylpiperidine are boiled together with 22 g of pulverized sodium amide in 300 ml of benzene, using a reflux condenser, while nitrogen is passed through the reaction mixture, until the evolution of ammonia has ceased. 64 g of benzyl chloride are then gradually added drop by drop to the boiling reaction product and boiling is continued for several hours. After having been cooled the solution is shaken with water and subsequently dried with potassium carbonate. The solvent having been evaporated the remaining base of 4-(N-phenyl-N-benzyl)-amino-1- methylpiperidine solidifies with the formation of crystals, the yield amounting to 123 g. The base is recrystallized from dibutyl ether and has a melting point of 115°C; its dihydrochloride melts at 189°C.

Therapeutic Function

Antihistaminic, Antiallergic

BAMIPINE 준비 용품 및 원자재

원자재

준비 용품


BAMIPINE 공급 업체

글로벌( 13)공급 업체
공급자 전화 이메일 국가 제품 수 이점
Shaanxi Didu New Materials Co. Ltd
+86-89586680 +86-13289823923
1026@dideu.com China 8722 58
Energy Chemical 021-58432009 400-005-6266
marketing@energy-chemical.com China 44941 58
Shaanxi DIDU pharmaceutical and Chemical Co., Ltd 17691182729 18161915376
1046@dideu.com China 10011 58

BAMIPINE 관련 검색:

BAMIPINE N-(1-ACETYL-2,3-DIHYDRO-(1H)-INDOL-5-YL)-N-(1-ACETYLPIPERIDIN-4-YL)BENZAMIDE 4-TERT-BUTYL-N-[2-METHYL-1H-INDOL-5-YL]-N-[1-(2-PHENYLETHYL)PIPERIDIN-4-YL]BENZAMIDE N-[1-(2,6-DIMETHOXYBENZYL)PIPERIDIN-4-YL]-N-PHENYL-3-(TRIFLUOROMETHYL)BENZAMIDE N-(1-BENZYLPIPERIDIN-4-YL)-N-(2-TERT-BUTYL-(1H)-INDOL-5-YL)-4-(METHYLSULPHONYL)BENZAMIDE N-(2-TERT-BUTYL-(1H)-INDOL-5-YL)-N-(1-PROPYLPIPERIDIN-4-YL)-3-(TRIFLUOMETHYL)BENZAMIDE N-(1-ACETYLPIPERIDIN-4-YL)-N-(2-TERT-BUTYL-(1H)-INDOL-5-YL)-4-(TRIFLUOROMETHYL)BENZAMIDE N-(1-ACETYL-2,3-DIHYDRO-(1H)-INDOL-5-YL)-N-(1-METHYLPIPERIDIN-4-YL)-4-(TRIFLUOROMETHYL)BENZAMIDE N-(1-ACETYL-2,3-DIHYDRO-(1H)-INDOL-5-YL)-N-[1-(2-PHENYLETHYL)PIPERIDIN-4-YL]BENZAMIDE N-(2-TERT-BUTYL-(1H)-INDOL-5-YL)-2-CHLORO-N-(1-PROPYLPIPERIDIN-4-YL)BENZAMIDE N-(1-BENZYLPIPERIDIN-4-YL)-N-(2-TERT-BUTYL-(1H)-INDOL-5-YL)-4-(TRIFLUOROMETHYL)BENZAMIDE N-(1-ACETYLPIPERIDIN-4-YL)-N-[3-[(TRIFLUOROMETHYL)SULPHONYL]PHENYL]BENZAMIDE N-(1-ACETYL-2,3-DIHYDRO-(1H)-INDOL-6-YL)-N-(1-METHYLPIPERIDIN-4-YL)-4-(TRIFLUOROMETHYL)BENZAMIDE N-(1-ACETYLPIPERIDIN-4-YL)-N-(2-TERT-BUTYL-(1H)-INDOL-5-YL)-4-(METHYLSULPHONYL)BENZAMIDE N-(1-ACETYLPIPERIDIN-4-YL)-N-(2-TERT-BUTYL-(1H)-INDOL-5-YL)-3,4,5-TRIMETHOXYBENZAMIDE N-(1-ACETYL-2,3-DIHYDRO-(1H)-INDOL-5-YL)-N-(1-ACETYLPIPERIDIN-4-YL)-4-(TRIFLUOROMETHYL)BENZAMIDE N-(1-ACETYL-2,3-DIHYDRO-(1H)-INDOL-5-YL)-N-(1-PROPYLPIPERIDIN-4-YL)3-(TRIFLUOROMETHYL)BENZAMIDE N-[2,3-DIHYDRO-1-(METHYLSULPHONYL)-(1H)-INDOL-5-YL]-N-(1-METHYLPIPERIDIN-4-YL)-3-(TRIFLUOROMETHYL)BENZAMIDE
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