ChemicalBook > CAS DataBase List > Verlukast

Verlukast

Product Name
Verlukast
CAS No.
120443-16-5
Chemical Name
Verlukast
Synonyms
019;L-668;L 668;MK 679;L 668019;Verlukast;R-(-)-MK 571;MK-0679 (Verlukast);3-[[(αR)-3-[(E)-2-(7-Chloro-2-quinolinyl)ethenyl]-α-(2-dimethylaminocarbonylethylthio)benzyl]thio]propionic acid;3-[[(R)-[3-[(1E)-2-(7-Chloro-2-quinolinyl)ethenyl]phenyl][[3-(dimethylamino)-3-oxopropyl]thio]methyl]thio]-propanoic Acid
CBNumber
CB51176855
Molecular Formula
C26H27ClN2O3S2
Formula Weight
515.09
MOL File
120443-16-5.mol
More
Less

Verlukast Property

Melting point:
57-62°C
Boiling point:
712.3±60.0 °C(Predicted)
Density 
1.327
storage temp. 
-20°C Freezer
solubility 
DMSO (Slightly), Methanol (Slightly, Heated, Sonicated), THF (Slightly, Sonicated)
form 
Solid
pka
4.27±0.10(Predicted)
color 
Light Yellow to Dark Yellow
More
Less

Hazard and Precautionary Statements (GHS)

More
Less

N-Bromosuccinimide Price

TRC
Product number
V128500
Product name
Verlukast
Packaging
10mg
Price
$130
Updated
2021/12/16
Biosynth Carbosynth
Product number
FV28691
Product name
Verlukast
Packaging
5mg
Price
$170
Updated
2021/12/16
Biosynth Carbosynth
Product number
FV28691
Product name
Verlukast
Packaging
10mg
Price
$270
Updated
2021/12/16
Biosynth Carbosynth
Product number
FV28691
Product name
Verlukast
Packaging
25mg
Price
$450
Updated
2021/12/16
Biosynth Carbosynth
Product number
FV28691
Product name
Verlukast
Packaging
50mg
Price
$700
Updated
2021/12/16
More
Less

Verlukast Chemical Properties,Usage,Production

Chemical Properties

Dark Yellow Solid

Originator

Verlukast,Merck Frosst (Merck and Co.)

Uses

A receptor antagonist for the treatment of respiratory diseases.

Manufacturing Process

5-(3-(2-(7-Chloroquinolin-2-yl)ethenyl)phenyl)-8-dimethylcarbamyl-4,6- dithiaoctanoic acid was prepared in 7 steps:
Step 1: Preparation of 2-bromomethyl-7-chloroquinoline:
A solution of 7-chloroquinaldine (177 g, 1 mole) N-bromosuccinimide (178 g, 1 mole), benzoylperoxide (1 g) in 2 L CCl 4 were heated at reflux for 2 days under a sun lamp. The reaction mixture was cooled, and passed through a plug of SiO 2 (approx. 1 Kg) using toluene as eluent. Chromatography on 2 x 1 kg SiO 2 columns using toluene as eluent afforded 110-120 g of the title compound, MP: 112°C.
Step 2: Preparation of (7-chloroquinolin-2-yl)-methyltriphenylphosphonium bromide:
To a suspension of 2-bromomethyl-7-chloroquinoline (120 g, 0.5 mol) in 800 ml of CH 3 CN at 60°C was added triphenylphosphine (183 g). The reaction mixture was heated overnight at 60°C, cooled and 400 ml ether was added. The solid was filtered and dried to yield 170 g phosphonium salt.
Step 3: Preparation of dimethyl 5-(3-formylphenyl)-4,6-dithianonanedioate:
To a solution of isophthalaldehyde (40 g, 0.3 mol.) in chloroform (400 ml) and methyl 3-mercaptopropanoate (68 ml, 0.6 mol) was added dropwise trimethylsilyl chloride (48 ml, 0.38 mol) over 30 min. The reaction mixture was stirred at room temperature for 2 hours. The reaction was quenched with 25% aq. NH 4 OAc, extracted with ethyl acetate, dried and evaporated. Flash chromatography of the residue afforded 50 g of the title compound.
Step 4: Preparation of dimethyl 5-(3-(2-(7-chloroquinolin-2- yl)ethenyl)phenyl)-4,6-dithianonanedioate:
To a suspension of 190 g phosphonium salt from Step 2 (0.36 mol.) in THF (2 L) at -78°C were added 1.6 M BuLi (220 ml) dropwise over 1.5 hrs. The resulting brown suspension was stirred 30 min at -78°C. To the suspension was added the aldehyde (Step 3) (11.7 g, 0.32 mol.) in THF (400 ml) dropwise over 1.5 hrs. The reaction mixture was allowed to warm to room temperature and quenched with pH 7 buffer (approx. 2 L). Ethyl acetate (1 L) was added. The organic phase was separated, dried and evaporated. Flash chromatography of the residue using 30% ethyl acetate hexane; followed by crystallization with 3:1 hexane/ether afforded 135 g of the title compound as a white solid. MP: 53°C.
Step 5: Preparation of methyl 5-(3-(2-(7-chloroquinolin-2-yl)ethenyl)phenyl)-8-dimethylcarbamyl-4,6-dithiaoctanoate:
A solution of the aluminum reagent was prepared by adding dropwise 150 ml of 2 M trimethylaluminum in hexane at -20°C to a solution of 2 M dimethylamine in toluene (300 ml). The solution was allowed to warm to room temperature. To the diester (step 4) (95 g) in CH 2 Cl 2 (1 L) was added dropwise 150 ml of the aluminum reagent. The reaction was stirred 7-8 hrs at room temperature. The reaction was carefully quenched at 0°C with 2 N HCl (until the vigorous reaction subsided); then pH 7 buffer (25% NH 4 OAc in H 2 O) (1 L) and CH 2 Cl 2 (1 L) were added. The organic phase was separated, dried and evaporated. Flash chromatography of the residue using first 50% ethyl acetate hexane followed by ethyl acetate afforded 38 g recovered di-ester and 38 g desired amide. The recovered di-ester was recycled through the sequence to give 18 g di-ester and 14 g desired amide. Total yield: 52 g of amide.
Step 6: Preparation of 5-(3-(2-(7-chloroquinolin-2-yl)ethenyl)phenyl)-8- dimethylcarbamyl-4,6-dithiaoctanoic acid:
To the amide (30 g) in 800 ml 1,2-dimethoxyethane (DME) was added 1.5 eq 1 N LiOH (75 ml). The reaction mixture was stirred one hour under N 2 . The DME was evaporated. The residue was partitioned between H 2 O (500 ml) and ethyl acetate (1 L). The aqueous phase was reextracted with ethyl acetate (500 ml). The aqueous phase was acidified with AcOH and a little 2 N HCl to pH 4 and extracted with ethyl acetate (2 x 600 ml). The organic phase was dried and evaporated. The residue was co-evaporated with toluene (300 ml) and triturated with cold ethyl acetate to give 18 g of the acid. MP: 153-155°C. Recrystallization from 2-butanone gave MP: 157-158°C.

Therapeutic Function

Anti-asthmatic, Antiallergic

Verlukast Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Verlukast Suppliers

Carbosynth
Tel
--
Fax
--
Email
sales@carbosynth.com
Country
United Kingdom
ProdList
6005
Advantage
58
More
Less

View Lastest Price from Verlukast manufacturers

Zhuozhou Wenxi import and Export Co., Ltd
Product
Verlukast 120443-16-5
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-07-10
Zhuozhou Wenxi import and Export Co., Ltd
Product
Verlukast 120443-16-5
Price
US $15.00-10.00/KG
Min. Order
1KG
Purity
99%+ HPLC
Supply Ability
Monthly supply of 1 ton
Release date
2021-07-09
Career Henan Chemical Co
Product
Verlukast 120443-16-5
Price
US $1.00/g
Min. Order
1g
Purity
99%
Supply Ability
1ton
Release date
2020-01-10

120443-16-5, VerlukastRelated Search:


  • 3-[[(R)-[3-[(1E)-2-(7-Chloro-2-quinolinyl)ethenyl]phenyl][[3-(dimethylamino)-3-oxopropyl]thio]methyl]thio]-propanoic Acid
  • L 668019
  • MK 679
  • R-(-)-MK 571
  • Verlukast
  • 3-[[(αR)-3-[(E)-2-(7-Chloro-2-quinolinyl)ethenyl]-α-(2-dimethylaminocarbonylethylthio)benzyl]thio]propionic acid
  • MK-0679 (Verlukast)
  • Propanoic acid, 3-[[(R)-[3-[(1E)-2-(7-chloro-2-quinolinyl)ethenyl]phenyl][[3-(dimethylamino)-3-oxopropyl]thio]methyl]thio]-
  • 019
  • L 668
  • L-668
  • 120443-16-5
  • C26H27ClN2O3S2
  • Intermediates & Fine Chemicals
  • Pharmaceuticals