pinazepam

pinazepam Basic information
Product Name:pinazepam
Synonyms:7-Chloro-1,3-dihydro-5-phenyl-1-(2-propynyl)-2H-1,4-benzodiazepin-2-one;Z-905;Zami-905;pinazepam;7-chloro-5-phenyl-1-prop-2-ynyl-3H-1,4-benzodiazepin-2-one;2H-1,4-Benzodiazepin-2-one, 7-chloro-1,3-dihydro-5-phenyl-1-(2-propyn-1-yl)-;pinazepam USP/EP/BP
CAS:52463-83-9
MF:C18H13ClN2O
MW:308.76
EINECS:257-934-9
Product Categories:Amines;Aromatics;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File:52463-83-9.mol
pinazepam Structure
pinazepam Chemical Properties
Melting point 140-142°
Boiling point 523.6±50.0 °C(Predicted)
density 1.2151 (rough estimate)
refractive index 1.5800 (estimate)
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pkapKa 2.34 (Uncertain)
color Off-White to Pale Beige
Stability:Light Sensitive
Safety Information
RIDADR 3249
HazardClass 6.1(b)
PackingGroup III
ToxicityLD50 in mice, rats (mg/kg): 1355, 5819 orally; 266, 622 i.p. (Scrollini, 1975); Also reported as LD50 in mice (mg/kg): 670 orally (Podesva, Vagi)
DEA Controlled SubstancesCSCN: 2883
CSA SCH: Schedule IV
NARC: No
MSDS Information
pinazepam Usage And Synthesis
OriginatorDomar ,Zambeletti, Italy,1975
UsesPinazepam is a is a benzodiazepine. Pinazepam possesses anxiolytic, anticonvulsant, sedative and skeletal muscle relaxant properties. Pinazepam is less toxic than Diazepam. This is a contolled substance (depressant). Anxiolytic.
DefinitionChEBI: Pinazepam is a benzodiazepine.
Manufacturing Process46.3 g (0.2 mol) of 2-amino-5-chlorobenzophenone were dissolved in 100 ml (1.28 mols) of propargyl bromide and the mixture refluxed for 4 hours. Thereafter, the whole was evaporated to dryness and the residue recrystallized from methanol to give 32.4 g (60.2%) of the desired 2-propargylamino-5chlorobenzophenone; melting point 92°C to 93°C.
2.7 g (0.01 mol) of the 2-propargylamino-5-chlorobenzophenone obtained as above and 2.23 g (0.01 mol) of phthalimidoacetyl chloride were added to 30 ml of chloroform and the whole was refluxed overnight. Thereafter, the reaction mixture was evaporated to dryness and the residue recrystallized from methanol to give 2.66 g (58.3%) of the desired 2-(Npropargyl)phthalimidoacetamide-5-chlorobenzophenone. Melting point: 176°C.
A suspension of 22.8 g (0.05 mol) of 2-(N-propargyl)-phthalimidoacetamido5-chlorobenzophenone in 250 ml ethanol containing 7.5 g hydrazine hydrate (0.15 mol) was heated under reflux for 2 hours, at the end of which time the reaction mixture was set aside overnight at ambient (25°C) temperature. Thereafter, the crystalline phthalyl hydrazide which had precipitated out was removed by filtration and washed with 3 x 50 ml aliquots of chloroform. The filtrate and washings were diluted with water and exhaustively extracted with chloroform. The chloroform extract was then evaporated and the residue washed with 100 ml hexane to promote crystallization. The crude 7-chloro-1propargyl-3H-1,4-benzodiazepine-2(1H)-one was recrystallized from a methanol-water mixture to give 10.5 g (71.4%) of the pure product. Melting point: 140°C to 142°C.
Therapeutic FunctionAntidepressant
pinazepam Preparation Products And Raw materials
Raw materialsPhthalimido Acetyl Chloride-->Hydrazine hydrate-->3-Bromopropyne-->2-Amino-5-chlorobenzophenone-->Nordazepam
pinazepam Nordazepam MEDAZEPAM 1-METHYL-5-PHENYL-1,3-DIHYDRO-BENZO[E][1,4]DIAZEPIN-2-ONE Diazapam PHENYL-PROP-2-YNYL-AMINE

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