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Brexpiprazole

CAS No.
913611-97-9
Chemical Name:
Brexpiprazole
Synonyms
OPC-34712;Brexpiprazole impurity a;7-[4-(4-(Benzo[b]thien-4-yl)-piperazin-1-yl)butoxy]-1H-quinolin-2-one;7-{4-[4-(1-Benzothiophen-4-yl)piperazin-1-yl]butoxy}quinolin-2(1H)-one;7-(4-(4-(Benzo[b]thiophen-4-yl)piperazin-1-yl)butoxy)quinolin-2(1H)-one;CS-1678;ipiprazole;Epiprazole;Brexpiprazole;Brexipiprazole
CBNumber:
CB52681994
Molecular Formula:
C25H27N3O2S
Molecular Weight:
433.57
MDL Number:
MFCD27987920
MOL File:
913611-97-9.mol
MSDS File:
SDS
Last updated:2024-04-02 22:45:52

Brexpiprazole Properties

Melting point 179 - 181oC
Boiling point 675.2±55.0 °C(Predicted)
Density 1.245±0.06 g/cm3(Predicted)
storage temp. Refrigerator
solubility Dichloromethane (Slightly), Chloroform (Slightly), Methanol (Slightly)
pka 11.22±0.70(Predicted)
form Solid
color White to Off-White
InChI InChI=1S/C25H27N3O2S/c29-25-9-7-19-6-8-20(18-22(19)26-25)30-16-2-1-11-27-12-14-28(15-13-27)23-4-3-5-24-21(23)10-17-31-24/h3-10,17-18H,1-2,11-16H2,(H,26,29)
InChIKey ZKIAIYBUSXZPLP-UHFFFAOYSA-N
SMILES N1C2=C(C=CC(OCCCCN3CCN(C4=C5C=CSC5=CC=C4)CC3)=C2)C=CC1=O
FDA UNII 2J3YBM1K8C
ATC code N05AX16

Brexpiprazole price More Price(29)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 22906 Brexpiprazole ≥98% 913611-97-9 10mg $44 2024-03-01 Buy
Cayman Chemical 22906 Brexpiprazole ≥98% 913611-97-9 50mg $130 2024-03-01 Buy
Cayman Chemical 22906 Brexpiprazole ≥98% 913611-97-9 100mg $235 2024-03-01 Buy
TRC B677385 Brexpiprazole 913611-97-9 500mg $415 2021-12-16 Buy
TRC B677385 Brexpiprazole 913611-97-9 5g $1075 2021-12-16 Buy
Product number Packaging Price Buy
22906 10mg $44 Buy
22906 50mg $130 Buy
22906 100mg $235 Buy
B677385 500mg $415 Buy
B677385 5g $1075 Buy

Brexpiprazole Chemical Properties,Uses,Production

Description

Brexpiprazole is a novel antipsychotic drug which serves as a serotonin ® dopamine activity modulator and has demonstrated efficacy as an adjunctive treatment in patients with major depressive disorder (MDD). The drug exhibits a unique pharmacological profile, acting as a partial agonist of serotonin 5-HT1A and dopamine D2 receptors and as a full antagonist of 5-HT2A and noradrenaline α1B/2C receptors, with similar subnanomolar binding affinity. The drug, which was developed by Otsuka and Lundbeck, was approved in 2015 by the FDA for the treatment of schizophrenia and as an adjunctive treatment for depression. Brexpiprazole is widely considered to be a successor to Otsuka’s antipsychotic drug aripiprazole (trade name Abilify) whose patent expired in August 2014.

Uses

Brexpiprazole is a kind of atypical antipsychotic. It is a dopamine D2 receptor partial agonist. As a novel serotonin-dopamine activity modulator, it can be used for the treatment of schizophrenia, and for the adjunctive treatment for depression. It can also provide efficacy and tolerability over established adjunctive treatments formajor depressive disorder(MDD).Recent study has also suggested it can ameliorate PCP-induced cognitive deficits in mice via 5-HT1A receptors.

Definition

ChEBI: Brexpiprazole(913611-97-9) is a N-arylpiperazine. It is a novel D2 dopamine and serotonin 1A partial agonist, called serotonin-dopamine activity modulator (SDAM), and a potent antagonist of serotonin 2A receptors, noradrenergic alpha 1B and 2C receptors. Brexpiprazole is a drug candidate useful in treatment and prevention of mental disorders including CNS disorders.

Synthesis

Commercially available fluorobenzaldehyde (60) underwent a substitution reaction with commercial tert-butyl piperazine-1- carboxylate (61) under basic conditions to afford the piperazinyl benzaldehyde 62 in excellent yield. Next, the construction of the benzothiophene was affected by initial condensation of thioglycolic acid ethyl ester 63 with ochlorobenzaldehyde 62 under mildly basic conditions at elevated temperatures. Treatment with aqueous base and adjustment of pH to roughly 5 through the use of 4 N HCl furnished the 2-carboxylic acid benzothiophene 64 in 80% yield across the three-step operation. Next, decarboxylation through the use of cuprous oxide using conditions slightly modified from those originally described by Goosen followed by acidic removal of the Boc protecting group on the terminal piperazine nitrogen secured the key piperazinyl benzothiophene subunit 65 as the corresponding hydrochloride salt.
The hydroxyquinolone and linker component synthesis began with alkylation of commercially available quinolone 66 with 1,4-bromochlorobutane (67) under basic conditions to furnish chloroalkoxyquinolone 68. A subsequent alkylation with hydrochloride salt 65 using potassium carbonate and warm aqueous ethanol followed by recrystallizative workup resulted in clean conversion to brexpiprazole (VIII) in 78% yield from 68.

Synthesis_913611-97-9

Enzyme inhibitor

This serotonin-dopamine activity modulator, or SDAM (FW = 433.60 g/mol; CAS 913611-97-9), also known as OPC-34712, Rexulti, 7-{4-[4-(1- benzothiophen-4-yl)piperazin-1-yl]butoxy}quinolin-2(1H)-one, is an atypical antipsychotic drug that acts as a dopamine D2L (Ki = 1.1 nM) and D3 (Ki = 0.3 nM) receptor partial agonist and a partial agonist of 5-HT1A receptors (Ki = 0.12 nM). Brexpiprazole is also an antagonist of the 5-HT2A (Ki = 0.47 nM), 5-HT2B (Ki = 1.9 nM), 5-HT7 (Ki = nM), α1B-adrenergic (Ki = 0.17 nM), α2C-adrenergic (Ki = 0.59 nM), and histamine H1 receptors (Ki = 19 nM). It has negligible affinity for the mACh receptors. Rexulti is an FDA-approved add-on medication for major depressive disorder in adults. See Aripiprazole

Mode of action

Brexpiprazole's suggested mechanism of action is based on its impact on dopamine and serotonin receptors. As a serotonin-dopamine activity modulator (SDAM), it acts as a novel partial agonist for D2 dopamine and serotonin 1A receptors while effectively blocking the serotonin 2A receptors, as well as noradrenergic alpha 1B and 2C receptors.

References

https://en.wikipedia.org/wiki/Brexpiprazole
https://www.drugbank.ca/drugs/DB09128
Maeda, K, et al. "Brexpiprazole I: in vitro and in vivo characterization of a novel serotonin-dopamine activity modulator." Journal of Pharmacology & Experimental Therapeutics 350.3(2014):589-604.
Maeda, K, et al. "Brexpiprazole II: antipsychotic-like and procognitive effects of a novel serotonin-dopamine activity modulator." Journal of Pharmacology & Experimental Therapeutics 350.3(2014):605.
Yoshimi, N, et al. "Effects of brexpiprazole, a novel serotonin-dopamine activity modulator, on phencyclidine-induced cognitive deficits in mice: a role for serotonin 5-HT1A receptors. " Pharmacology Biochemistry & Behavior 124(2014):245.

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Related articles

View Lastest Price from Brexpiprazole manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Brexpiprazole pictures 2024-04-25 Brexpiprazole
913611-97-9
US $1.00 / g 1g 99% 100kg Dorne Chemical Technology co. LTD
Brexpiprazole pictures 2024-04-12 Brexpiprazole
913611-97-9
US $3.00-1.00 / kg 1kg 99.9% 10 tons Shanghai Aosiris new Material Technology Co., LTD
Brexpiprazole pictures 2024-04-12 Brexpiprazole
913611-97-9
US $0.00 / kg 1kg 0.99 10T Shandong Hanjiang Chemical Co., Ltd
  • Brexpiprazole pictures
  • Brexpiprazole
    913611-97-9
  • US $1.00 / g
  • 99%
  • Dorne Chemical Technology co. LTD
  • Brexpiprazole pictures
  • Brexpiprazole
    913611-97-9
  • US $3.00-1.00 / kg
  • 99.9%
  • Shanghai Aosiris new Material Technology Co., LTD
  • Brexpiprazole pictures
  • Brexpiprazole
    913611-97-9
  • US $0.00 / kg
  • 0.99
  • Shandong Hanjiang Chemical Co., Ltd

Brexpiprazole Spectrum

Brexpiprazole 7-[4-(4-benzo[b]thien-4-yl-1-piperazinyl)butoxy]- 2(1H)-Quinolinone 7-[4-[4-(1-Benzothiophen-4-yl)piperazin-1-yl]butoxy]-1H-quinolin-2-one CS-1678 OPC 34712; OPC34712; OPC-34712 Brexpiprazole(OPC34712) OPC-34712;OPC34712 2(1H)-Quinolinone, 7-[4-(4-benzo[b]thien-4-yl-1-piperazinyl)butoxy]- Epipiprazole Impurities Epipiprazole863 Epipiprazole864 Epipiprazole860 Impurities of Epipiprazole1 BrexpiprazoleQ: What is Brexpiprazole Q: What is the CAS Number of Brexpiprazole Q: What is the storage condition of Brexpiprazole TIANFU CHEM---Brexpiprazole 7-(4-(4-(Benzo[b]thiophen-4-yl)piperazin-1-yl)butoxy)quinolin-2(1H)-one Brexpiprazole impurity a 7-{4-[4-(1-Benzothiophen-4-yl)piperazin-1-yl]butoxy}quinolin-2(1H)-one OPC-34712 7-[4-(4-(Benzo[b]thien-4-yl)-piperazin-1-yl)butoxy]-1H-quinolin-2-one 7-[4-[4-(4-Benzothienyl)-1-piperazinyl]butoxy]quinolin-2(1H)-one Brexpiprazole Crude Brexpiprazole 7-[4-(4-Benzo[b]thien-4-yl-1-piperazinyl)butoxy]-2(1H)- quinolinone ipiprazole Epiprazole Brexipiprazole 913611-97-9 Dopamine D2 receptor partial agonist API Inhibitors 913611-97-9