5-(2-Fluorphenyl)-1,3-dihydro-1-methyl-7-nitro-2H-1,4-benzodiaze-pin-2-on

Gefahreninformationscode (GHS)

• Bildanzeige (GHS)

  

• Alarmwort

  Warnung

• Gefahrenhinweise

  H302：Gesundheitsschädlich bei Verschlucken.

  H319：Verursacht schwere Augenreizung.

• Sicherheit

  P305+P351+P338：BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach Möglichkeit entfernen. Weiter spülen.

FLUNITRAZEPAM Chemische Eigenschaften,Einsatz,Produktion Methoden

• R-Sätze Betriebsanweisung:

  R22:Gesundheitsschädlich beim Verschlucken.
  R36:Reizt die Augen.
  R39/23/24/25:Giftig: ernste Gefahr irreversiblen Schadens durch Einatmen, Berührung mit der Haut und durch Verschlucken.
  R23/24/25:Giftig beim Einatmen, Verschlucken und Berührung mit der Haut.
  R11:Leichtentzündlich.

• S-Sätze Betriebsanweisung:

  S7:Behälter dicht geschlossen halten.
  S16:Von Zündquellen fernhalten - Nicht rauchen.
  S36/37:Bei der Arbeit geeignete Schutzhandschuhe und Schutzkleidung tragen.
  S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).
  S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
  S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.

• Chemische Eigenschaften

  White or yellowish, crystalline powder.

• Originator

  Roipnol,Roche,Italy,1976

• Verwenden

  antitussive

• Verwenden

  Flunitrazepam is used as an hypnotic. This is a controlled substance (depressant).

• Definition

  ChEBI: Flunitrazepam is a 1,4-benzodiazepinone that is nitrazepam substituted by a methyl group at position 1 and by a fluoro group at position 2'. It is a potent hypnotic, sedative, and amnestic drug used to treat chronic insomnia. It has a role as a sedative, a GABAA receptor agonist and an anxiolytic drug. It is a 1,4-benzodiazepinone, a C-nitro compound and a member of monofluorobenzenes.

• Manufacturing Process

  A mixture of 176 grams of orthofluorobenzoyl chloride and 64 grams of parachloroaniline was stirred and heated to 180°C, at which temperature 87 grams of zinc chloride was introduced, the temperature raised to 200° to 205°C and maintained there for 40 minutes. The golden colored melt was quenched by the careful addition of 500 ml of 3 N hydrochloric acid and the resulting mixture refluxed for 5 minutes. The acid solution was decanted and the process repeated three times to remove all orthofluorobenzoic acid. The grey granular residue was dissolved in 300 ml of 75% (v/v) sulfuric acid and refluxed for 40 minutes to complete hydrolysis. The hot solution was poured over 1 kg of ice and diluted to 2 liters with water. The organic material was extracted with four 300 ml portions of methylene chloride, and the combined extracts subsequently washed with two 500 ml portions of 3 N hydrochloric acid to remove traces of para-chloroaniline, three 500 ml portions of 5 N sodium hydroxide solution to remove orthofluorobenzoic acid, and finally two 200 ml portions of saturated brine solution.
  The combined methylene chloride extracts were dried over anhydrous sodium sulfate and the solvent removed to give the crude 2-amino-5-chloro-2'- fluorobenzophenone which upon recrystallization from methanol formed yellow needles melting at 94° to 95°C.
  50.0 grams of 2-amino-5-chloro-2'-fluorobenzophenone in 300 cc of tetrahydrofuran was hydrogenated at atmospheric pressure in the presence of 10 grams of charcoal (Norite), 30.0 grams of potassium acetate and 2.5 cc of a 20% palladous chloride solution (20% by weight of palladium). After an initiation period varying from 10 minutes to an hour, hydrogen uptake was rapid and stopped completely after the absorption of the theoretical amount.
  Filtration of the catalyst over a Hyflo pad and removal of the solvent left a yellow crystal line residue. The crude mixture of ketone and potassium acetate was partitioned between methylene chloride (300 cc) and water (1 liter). The layers were separated and the water layer washed with methylene chloride (3 x 50 cc). The organic layers were combined, washed with 3 N sodium hydroxide solution (2 x 50 cc), water (3 x 100 cc), dried over anhydrous sodium sulfate and filtered. The solvent was removed and the product recrystallized from ethanol to give 2-amino-2'-fluorobenzophenone as yellow prisms melting at 126° to 128°C.
  A solution of 21.5 grams of 2-amino-2'-fluorobenzophenone in 500 cc of ether was treated with 20 cc of a 20% (v/v) solution of bromoacetyl bromide in ether. The mixture was shaken and allowed to stand for 5 minutes and then washed with water (20 cc). The process was repeated five times. The final solution was washed thoroughly with water (5 x 500 cc) and concentrated to 100 cc. The crystals were filtered and recrystallized from methanol to give 2- bromacetamido-2'-fluorobenzophenone as white needles melting at 117° to 118.5°C.
  A solution of 23.7 grams of 2-bromoacetamido-2'-fluorobenzophenone in tetrahydrofuran (100 cc) was added to liquid ammonia (approximately 500 cc) and allowed to evaporate overnight. The residue was treated with water (1 liter) and the crystals filtered off and refluxed in toluene (100 cc) for 30 minutes. The mixture was treated with decolorizing carbon (Norite) and filtered over Hyflo. The solution was concentrated to a small volume (25 cc) cooled, diluted with 20 cc of ether and allowed to stand. The product was recrystallized from acetone/hexane to give 5-(2-fluorophenyl)-3H-1,4- benzodiazepin-2(1H)-one as white needles melting at 180° to 181°C.
  23.8 grams of 5-(2-fluorophenyl)-3H-1,4-benzodiazepin-2(1H)-one was dissolved in 50 cc of concentrated sulfuric acid at 0°C. To the resulting mixture there was then added dropwise with stirring a solution of 7.1 grams of potassium nitrate in 20 cc of concentrated sulfuric acid. The mixture was stirred for 2? hours at 0°C and then diluted with 300 grams of ice. The r

• Trademarks

  Rohypnol (Roche, Puerto Rico);Darkene;Flumipam;Hipnosedon;Hiposedon;Hypnodorm;Hypnosedon;Libelins;Noviel;Primun;Riopnol;Rohipnol;Rohpinol;Rohpnol;Valseram.

• Therapeutic Function

  Hypnotic

• Weltgesundheitsorganisation (WHO)

  Flunitrazepam, a benzodiazepine derivative with sedative and hypnotic activity, was introduced in 1974 for the management of anxiety. Although it is subject to international control under Schedule IV of the 1971 Convention on Psychotropic Substances, its potential for abuse by drug addicts has led at least two countries (Germany and Turkey) to apply controls equivalent to those of Schedule II. (Reference: (UNCPS4) United Nations Convention on Psychotropic Substances (IV), , , 1971)

• Biochem/physiol Actions

  Hypnotic; anxiolytic; ligand for the GABAA receptor benzodiazepine modulatory site.

FLUNITRAZEPAM Upstream-Materialien And Downstream Produkte

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