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Pipenzolate bromide

Chemical Name 1-ethyl-3-[(hydroxydiphenylacetyl)oxy]-1-methylpiperidinium bromide Common Name N-ethyl-3-piperidyl benzilate methobromide [Pg.1243]

Merrell National Roger Bellon Panthox Burck [Pg.1243]

N-Ethyl-3-chloropiperidine Benzilic acid Methyl bromide [Pg.1243]

N-ethyl-3-chloropiperidine was prepared according to the method of Fuson and Zirkle described in Volume 70, J. Am. them. Soc., p 2760. 12.0 g (0.0B1 mol) of N-ethyl-3-chloropiperidine was mixed with 1B.6 g (0.0B1 mol) of benzilic acid and 80 cc of anhydrous isopropyl alcohol as a solvent. The mixture was refluxed for 72 hours. The solution was then filtered and concentrated at 30 mm of mercury. The concentrate was dissolved in water, acidified with hydrochloric acid and extracted with ether to remove the unreacted benzilic acid. [Pg.1243]

The aqueous layer was neutralized with sodium bicarbonate and the product was extracted with ether. The ethereal solution of the product was dried with potassium carbonate, the ether was removed by distillation and the residue was distilled at 0.12 to 0.1B mm of mercury, the BP being 194° to 19B°C. A yield of 16.5 g (60% of theoretical) of N-ethyl-3-piperidyl-benzllate was obtained. [Pg.1243]

Minamr, S., IWatsumoto, J.-l., Kawaguchi, K., Mishio, S., Shimizu, M., Takase, Y, and Nakamura, S. U.S. Patent 3,887,557 June 3, 1975 assigned to Dainippon Pharma-ceuticai Co. Ltd., Japan [Pg.1243]

N-Ethyl-3 hloropiperidine Benzilic acid Methyl bromide [Pg.1243]

Chemical Name 1-ethYl-3-[(hydroxYdiphenYlacetYl)oxYl-l-methylpiperidinium bromide Common Name N-ethYi-3-piperidYi benzilate methobromide Structurai Formuia  [Pg.1243]

N-Ethyl-3-ohloropiperidine Benzilic acid Methyl bromide [Pg.1243]

Mepenzolate bromide Pipenzolate bromide Pipoxolan HCI Benzoic anhydride Flavoxate HCI Benzonitrile Fentiazac Benzophenone Diphenidol Phenytoin 1,4-Benzoaquinone Dobesilate calcium Ethamsylate Megestrol acetate Benzotetronic acid... [Pg.1615]

N-Ethyl-3-chloropiperidine Pipenzolate bromide 1 -Ethyl-3-chloropyrrolidine Doxapram HCI Ethyl -chlorovinyl ketone Ethchlorvynol Ethyl cyanoacetate Ethosuximide Piprozolin Tinoridine... [Pg.1633]

C,4H 203 76-93-7) see Hutropium bromide Mepenzolate bromide Pipenzolate bromide Pipoxolan Propiverine benziiic chloride... [Pg.2301]

C21H2SNO2 3567-/2-2) see Pipenzolate bromide 3emfo-a-hydroxy-a-phenylbenzeneacetic acid 6-methoxy-8-methyl-8-azabicyclo[3.2.1]oct-3-yl ester (C23H27NO4) see Tropenziline bromide a-hydroxy-a-phenylbenzeneacetic acid l-methyl>4-piperi-dinyl ester... [Pg.2399]

Pipe materials, types of, 19 476-478 Pipenzolate bromide, 4 360t Pipe provers, 11 652-653 Piperack(s), 19 494 multielevation, 19 515 in plant layout, 19 515-519 Piperack configurations, types of, 19 516 Piperazine, 3 485... [Pg.710]

C21H25NO, 3567-12-2) sec Pipenzolate bromide 3em/Tropenziline bromide tx-hydroxy-a-phenylbenzcneacetic acid l-methyl-4-piperi-dinyl ester... [Pg.2399]

Acepifylline Pipenzolate Bromide Propantheline Bromide Pyridostigmine Bromide... [Pg.1094]

CD. 18 F Irritable behavior. Had received pipenzolate bromide, promezathine hydrochloride, and dicylcomine intermittently. Urinary catecholamines transiently increased. 3830 U/liter Bone 6... [Pg.180]

See other pages where Pipenzolate bromide is mentioned: [Pg.766]    [Pg.1243]    [Pg.1243]    [Pg.1730]    [Pg.1730]    [Pg.1649]    [Pg.1649]    [Pg.2377]    [Pg.2413]    [Pg.300]    [Pg.766]    [Pg.2762]    [Pg.2762]    [Pg.1649]    [Pg.1649]    [Pg.2413]    [Pg.905]    [Pg.905]    [Pg.1082]    [Pg.1089]    [Pg.1130]    [Pg.1150]    [Pg.1156]    [Pg.1543]    [Pg.222]    [Pg.1243]    [Pg.1243]    [Pg.1730]    [Pg.1730]    [Pg.1243]    [Pg.1243]   
See also in sourсe #XX -- [ Pg.1649 ]



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