ChemicalBook--->CAS DataBase List--->514-65-8

514-65-8

514-65-8 Structure

514-65-8 Structure
IdentificationBack Directory
[Name]

Bipariden
[CAS]

514-65-8
[Synonyms]

kl373
KL 373
Akineton
Akinophyl
bipariden
Bibristan
Beperiden
biperiden
Biperidine
BiperidenHcl
Biperiden, USP
BIPERIDEN (200 MG)
Bipariden USP/EP/BP
Biperiden Hydrochloride USP
Biperiden Hcl -USP/ EP/IP/JP
3-Piperidino-1-phenyl-1-bicyclo-
Biperiden (Mixture of diastereomers)
-5-Norbornen-2-yl-phenyl-1-piperidinepropanol
3-Piperidino-1-phenyl-1-bicycloheptenyl-1-propanol
1-Bicycloheptenyl-1-phenyl-3-piperidino-propanol-1
alpha-5-norbornen-2-yl-alpha-phenyl-1-piperidinepropano
alpha-5-Norbornen-2-yl-alpha-phenyl-1-piperidinepropanol
-Bicyclo[2,2,1]hept-5-en-2yl-phenyl-1-piperidinepropanol
1-Piperidinepropanol, alpha-5-norbornen-2-yl-alpha-phenyl-
a-bicyclo[2.2.1]hept-5-en-2yl-a-phenyl-1-piperidinepropanol
alpha-phenyl-alpha-(2-piperidinoethyl)-5-norbornene-2-methano
1-Piperidinepropanol, α-bicyclo[2.2.1]hept-5-en-2-yl-α-phenyl-
1-Piperidinepropanol, a-bicyclo[2.2.1]hept-5-en-2-yl-a-phenyl-
α-(Bicyclo[2.2.1]hept-5-en-2-yl)-α-phenyl-1-piperidinopropanol
5-Norbornene-2-methanol, alpha-phenyl-alpha-(2-piperidinoethyl)-
1-phenyl-3-piperidino-1-(8,9,10-trinorborn-5-en-2-yl)propan-1-ol
3-Piperidino-1-phenyl-1-bicyclo(2.2.1)hepten-(5)-yl-propanol-(1)
α-(Bicyclo[2.2.1]hept-5-en-2-yl)-α-phenyl-1-piperidine-1-propanol
1-Piperidinepropanol, a-5-norbornen-2-yl-a-phenyl- (6CI, 7CI, 8CI)
1-(5-bicyclo[2.2.1]hept-2-enyl)-1-phenyl-3-(1-piperidyl)propan-1-ol
alpha-bicyclo(2.2.1)hept-5-en-2-yl-alpha-phenyl-1-piperidinepropano
1-Bicyclo[2.2.1]hept-5-en-2-yl-1-phenyl-3-(1-piperidinyl)-1-propanol
1-Piperidinepropanol, alpha-bicyclo[2.2.1]hept-5-en-2-yl-alpha-phenyl-
alpha-(bicyclo(2.2.1)hept-5-en-2-yl)-alpha-phenyl-1-piperidinopropanol
alpha-(Bicyclo(2.2.1)hept-5-en-2-yl)-alpha-phenyl-1-piperidino propanol
Alpha-5-Norbornene-2-yl-alphaphentl-1-piperidinepropanol (Biperiden base)
Bicyclo[2.2.1]hept-5-ene-2-methanol, alpha-phenyl-alpha-[2-(1-piperidinyl)ethyl]-
[EINECS(EC#)]

208-184-6
[Molecular Formula]

C21H29NO
[MDL Number]

MFCD05662335
[MOL File]

514-65-8.mol
[Molecular Weight]

311.47
Chemical PropertiesBack Directory
[Melting point ]

114°C
[Boiling point ]

451.49°C (rough estimate)
[density ]

1.0202 (rough estimate)
[refractive index ]

1.5614 (estimate)
[storage temp. ]

2-8°C
[solubility ]

Chloroform (Slightly), DMSO (Slightly,Sonicated), Methanol (Slightly, Sonicated)
[form ]

Solid
[pka]

14.05±0.29(Predicted)
[color ]

White to Off-White
[Water Solubility ]

25.1 mg/L
[NIST Chemistry Reference]

Biperiden(514-65-8)
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Magnesium-->Hydrochloric acid-->Acetophenone-->Formaldehyde
Safety DataBack Directory
[Hazardous Substances Data]

514-65-8(Hazardous Substances Data)
[Toxicity]

LD50 in mice (mg/kg): 195 s.c., 56 i.v. (Klavehn)
Hazard InformationBack Directory
[Chemical Properties]

Crystals. Melting point 112-116°C (101°C). Sparingly soluble in water, slightly soluble in ethanol, and freely soluble in methanol. Its hydrochloride (C????H????NO·HCl), also known as Akineton (Akinophyl), appears as white crystals. It decomposes at approximately 275°C, although its melting point has also been reported to be 238°C.
[Originator]

Akineton HCl,Knoll,US,1959
[Uses]

amoebicide
[Definition]

ChEBI: N-Propylpiperidine in which the methyl hydrogens are substituted by hydroxy, phenyl, and 5-norbornen-2-yl groups. A muscarinic antagonist affecting both the central and peripheral nervous systems, it is used in the treatment of all form of Parkinson's disease.
[Manufacturing Process]

65 grams of 3-piperidino-1-phenyl propanone-1 of the summary formula C14H29ON, produced according to Mannich's reaction by reacting acetophenone with formaldehyde and piperidine hydrochloride are dissolved in 300 cc of benzene. The resulting solution is added to an organo-magnesium solution prepared from 96 grams of [δ5-bicyclo-(2,2,1)-heptenyl-2]-chloride (also known as 5-chloro-2-norbomene) 18.5 grams of magnesium shavings, and 300 cc of ether.
The reaction mixture is boiled for half an hour under reflux. Thereafter the ether is removed by distillation, until the inside temperature reaches 65°- 70°C. The resulting benzene solution is added to 95 cc concentrated hydrochloric acid containing ice for further processing. Thereby, 3-piperidino- 1-phenyl-1-[δ5-bicyclo-(2,2,1)-heptenyl-2]-propanol-1 of the summary formula C21H29ON is obtained. The compound melts at 101°C and its chlorohydrate has a melting point of about 238°C. The compound is difficultly soluble in water, slightly soluble in ethanol, and readily soluble in methanol.
[Brand name]

Akineton (Abbott).
[Therapeutic Function]

Antiparkinsonian
[General Description]

Biperiden,α-5-norbornen-2-yl- -phenyl-1-piperidinepropanol (Akineton), introduced in 1959,has a relatively weak visceral anticholinergic, but a strongnicotinolytic, action in terms of its ability to block nicotineinducedconvulsions. Therefore, its neurotropic action israther low on intestinal musculature and blood vessels. It hasa relatively strong musculotropic action, which is aboutequal to that of papaverine, in comparison with most syntheticanticholinergic drugs. Its action on the eye, althoughmydriatic, is much lower than that of atropine. These weakanticholinergic effects add to its usefulness in Parkinson syndromeby minimizing side effects.
[Clinical Use]

Biperiden is used in all types of Parkinson disease (postencephalitic,idiopathic, arteriosclerotic) and helps toeliminate akinesia, rigidity, and tremor. It is also usedin drug-induced extrapyramidal disorders to eliminatesymptoms and permit continued use of tranquilizers.Biperiden is also of value in spastic disorders not related toparkinsonism, such as multiple sclerosis, spinal cord injury,and cerebral palsy. It is contraindicated in all formsof epilepsy.
[Safety Profile]

Poison by ingestion,subcutaneous, intraperitoneal, and intravenous routes.When heated to decomposition, it emits toxic fumes ofNOx.
[Synthesis]

Biperiden, 1-(5-norbornen-2-yl)-1-phenyl-3-piperidinopropan-1-ol (10.2.4), is also synthesized according to the method of making trihexyphenidyl, except by reacting 2-(1-piperidino)propiophenone (10.2.1) with 5-norbornen-2-ylmagnesiumbromide [33,34].
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