Bupropion
- Product Name
- Bupropion
- CAS No.
- 34911-55-2
- Chemical Name
- Bupropion
- Synonyms
- BUPROPION HCL;AMFEBUTAMONE;Amfebutamon;ZYNTABAC;Bupropion;AMFEBUTAMONE HCL;Bupropion 34911-55-2;Wellbatrin：Wellbutrin;BUPROPION/AMFEBUTAMONE;Bupropion controlled release
- CBNumber
- CB8140067
- Molecular Formula
- C13H18ClNO
- Formula Weight
- 239.74
- MOL File
- 34911-55-2.mol
Bupropion Property
- Melting point:
- 233-234°C
- Boiling point:
- bp.005 52°
- Density
- 1.066±0.06 g/cm3(Predicted)
- solubility
- ethanol: 193 mg/mL solutions may be stored for several days at 4 °C.
- form
- solid
- pka
- pKa 7.0 (Uncertain)
- color
- white
- BCS Class
- 1
- CAS DataBase Reference
- 34911-55-2(CAS DataBase Reference)
- EPA Substance Registry System
- 1-Propanone, 1-(3-chlorophenyl)-2-[(1,1-dimethylethyl)amino]- (34911-55-2)
Safety
- Hazard Codes
- Xn
- Risk Statements
- 22
- Safety Statements
- 36
- WGK Germany
- 3
- RTECS
- UG8858000
- HazardClass
- IRRITANT
- Hazardous Substances Data
- 34911-55-2(Hazardous Substances Data)
N-Bromosuccinimide Price
- Product number
- 047881
- Product name
- Bupropion hydrochloride
- Purity
- 95+%
- Packaging
- 5g
- Price
- $245
- Updated
- 2021/12/16
- Product number
- 8068AH
- Product name
- Bupropion
- Packaging
- 5g
- Price
- $380
- Updated
- 2021/12/16
- Product number
- API0008795
- Product name
- BUPROPION
- Purity
- 95.00%
- Packaging
- 1G
- Price
- $675.68
- Updated
- 2021/12/16
- Product number
- 047881
- Product name
- Bupropion hydrochloride
- Purity
- 95+%
- Packaging
- 25g
- Price
- $735
- Updated
- 2021/12/16
- Product number
- 047881
- Product name
- Bupropion hydrochloride
- Purity
- 95+%
- Packaging
- 1g
- Price
- $82
- Updated
- 2021/12/16
Bupropion Chemical Properties,Usage,Production
Description
Bupropion hydrochloride, an aminoketone structurally unrelated to tricyclics or tetracyclics, is a dopamine uptake blocker with antidepressant activity. Its clinical efficacy is reportedly comparable to that of amitriptyline, yet unlike most conventional antidepressants, bupropion hydrochloride is not associated with orthostatic hypotension or other cardiovascular side-effects.
Originator
Burroughs Wellcome (United Kingdom)
Uses
vasoconstrictor;non-selective agonist of all adrenergic receptors
Uses
Bupropion Hydrochloride used in methods of treating sleep disorders associated with pain.
Definition
ChEBI: Bupropion is an aromatic ketone that is propiophenone carrying a tert-butylamino group at position 2 and a chloro substituent at position 3 on the phenyl ring. It has a role as an antidepressant, an environmental contaminant and a xenobiotic. It is a secondary amino compound, a member of monochlorobenzenes and an aromatic ketone.
Manufacturing Process
To ethyl magnesium bromide (2 L, 3 M) was added over 45 min with stirring
and cooling m-chlorobenzonitrile (688.0 g, 5 mole) in ether (2.5 L). The
resultant solution was heated under gentle reflux for 5 h. The reaction mixture
was hydrolyzed with cold dilute hydrochloric acid, the ether was distilled off,
and the aqueous solution was heated at 90°C for 1 h. The flask was then
cooled. The solid ketone that separated was washed with cold water and
recrystallized from methanol. The recrystallized m-chloropropiophenone,
melting point 39°-40°C, weighed 750.0 g.
In methylene chloride (3 L) was dissolved m-chloropropiophenone (698.0 g;
4.15 mole). The solution was stirred with charcoal (Darco) and magnesium
sulfate for 2 h and filtered. To it was added with stirring (662.0 g) of bromine
in methylene chloride (1 L). When the bromine color had faded completely,
the solvent was evaporated in vacuum and m-chloro-α-bromopropiophenone
was obtained as oil.
The m-chloro-α-bromopropiophenone was dissolved in acetonitrile (1300 ml).
To this, t-butylamine (733.0 g) in acetonitrile (1300 ml) was added while
keeping the temperature below 32°C. The reaction mixture was allowed to
stand over night. It was then partitioned between water (4200 ml) and ether
(2700 ml). The aqueous layer was extracted with a further portion of ether
(1300 ml). The combined ethereal layers were then washed with water (4200
ml) to which hydrochloric acid was added until the pH of the aqueous layer
was 9. The aqueous layer was separated and washed with ether (500 ml) and
then discarded. The combined ethereal layers were then stirred with ice
(560.0 g) and concentrated hydrochloric acid (324 ml). The ethereal layer was
separated and again washed with water (200 ml) and concentrated
hydrochloric acid (50 ml). These last two acid layers were combined and
concentrated in vacuum until crystals appeared. The solution was then chilled
to 5°C and filtered. The product was sucked dry, washed with acetone and
recrystallized from a mixture of isopropanol (3 L) and absolute ethanol (800
ml). The DL-m-chloro-α-t-butylaminopropiophenone hydrochloride so was
obtained, melting point 233°-234°C.
The DL-m-chloro-α-t-butylaminopropiophenone was obtained by treatment of
DL-m-chloro-α-t-butylaminopropiophenone hydrochloride with sodium
hydroxide.
brand name
Wellbutrin (GlaxoSmithKline); Zyban (GlaxoSmithKline).
Therapeutic Function
Antidepressant; Smoking cessation aid
Biological Functions
Bupropion (Wellbutrin) is a pharmacologically unique antidepressant, since it is a weak inhibitor of both dopamine and norepinephrine neuronal reuptake. However, its actual antidepressant activity is not well understood. Bupropion is generally well tolerated and does not block muscarinic, histaminergic, or adrenergic receptors. Unlike the SSRIs and venlafaxine, bupropion does not cause sexual side effects. However, it can cause CNS stimulation, including restlessness and insomnia. High doses of bupropion, given as its original formulation, were associated with a risk of seizures in 0.4% of patients. However, this risk is lower with slow-release bupropion (Wellbutrin SR). This formulation still requires dosing twice a day, and bupropion is contraindicated in patients with a history of seizures. Bupropion inhibits the cytochrome P450 2D6 isoenzyme and may elevate blood levels of drugs metabolized by this route.
General Description
The mechanism of action of bupropion (Wellbutrin) is consideredcomplex and reportedly involves a block of DA reuptakevia the dopamine transporter (DAT), but the overallantidepressant action is noradrenergic. A metabolite thatcontributes to the overall action and its formation can beeasily rationalized. Oxidation of one of the methyl groupson the t-butyl substituent yields hydroxybupropion, an activemetabolite. Reduction of the keto group also occurs,yielding threohydrobupropion and erythrohydrobupropion.Both of these metabolites are also active.
Hydroxybupropion is half as potent as the parent bupropion,and the hydrobupropion isomers are five times less potent.The presence of these metabolites, especially hydroxybupropionwhich is formed by cytochrome P450 2D6(CYP2D6), suggests that there will be a myriad of drug interactionswith bupropion.
Pharmacology
Bupropion is an α-aminoketone that is structurally related to amphetamines, and it exhibits unique activity comparable to that of other antidepressants. It is believed that bupropion restores the total amount of norepinephrine in the body. This compound is a poor reuptake inhibitor of dopamine, and does not exhibit anticholinergic activity or inhibit MAO. Its efficacy as an antidepressant is comparable to that of tricyclic antidepressants, and as a serotonin uptake inhibitor it is comparable to fluoxetine.
Synthesis
The synthesis of bupropion, 1-3(-chlorophenyl)-2-[(1,1-dimethylethyl)amino]- 1-propanone (7.3.5), begins with the reaction of 3-chlorobenzonitrile, with ethylmagnesium bromide to give 3-chloropropiophenone (7.3.3). Brominating this with bromine gives 3-chloro-|á-bromopropiophenone (7.3.4), which on reaction with tert-butylamine gives bupropion (7.3.5) [54¨C58].
Bupropion Preparation Products And Raw materials
Raw materials
Preparation Products
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