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Nemorexant

Product Name
Nemorexant
CAS No.
1505484-82-1
Chemical Name
Nemorexant
Synonyms
Daridorexant;Nemorexant;Daridorexant,Nemorexant;emorexant, Daridorexant;(S)-[2-(6-Chloro-7-methyl-2-benzimidazolyl)-2-methyl-1-pyrrolidinyl][5-methoxy-2-(2H-1,2,3-triazol-2-yl)phenyl]methanone;(2S)-2-(6-Chloro-7-methyl-1H-benzimidazol-2-yl)-2-methyl-1-pyrrolidinyl][5-methoxy-2-(2H-1,2,3-triazol-2-yl)phenyl]methanone;(S)-(2-(6-chloro-7-methyl-1H-benzo[d]imidazol-2-yl)-2-methylpyrrolidin-1-yl)(5-methoxy-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone;Methanone, [(2S)-2-(6-chloro-7-methyl-1H-benzimidazol-2-yl)-2-methyl-1-pyrrolidinyl][5-methoxy-2-(2H-1,2,3-triazol-2-yl)phenyl]-
CBNumber
CB04796673
Molecular Formula
C23H23ClN6O2
Formula Weight
450.92
MOL File
1505484-82-1.mol
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Nemorexant Property

Boiling point:
747.6±70.0 °C(Predicted)
Density 
1.42±0.1 g/cm3(Predicted)
storage temp. 
Store at -20°C
solubility 
DMSO : ≥ 250 mg/mL (554.42 mM)
pka
10.47±0.30(Predicted)
InChIKey
NBGABHGMJVIVBW-QHCPKHFHSA-N
SMILES
C(N1CCC[C@]1(C1NC2=C(C)C(Cl)=CC=C2N=1)C)(C1=CC(OC)=CC=C1N1N=CC=N1)=O
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

ChemScene
Product number
CS-0039396
Product name
Nemorexant
Purity
99.56%
Packaging
1mg
Price
$100
Updated
2021/12/16
ChemScene
Product number
CS-0039396
Product name
Nemorexant
Purity
99.56%
Packaging
5mg
Price
$320
Updated
2021/12/16
ChemScene
Product number
CS-0039396
Product name
Nemorexant
Purity
99.56%
Packaging
10mg
Price
$530
Updated
2021/12/16
ChemScene
Product number
CS-0039396
Product name
Nemorexant
Purity
99.56%
Packaging
25mg
Price
$1050
Updated
2021/12/16
ChemScene
Product number
CS-0039396
Product name
Nemorexant
Purity
99.56%
Packaging
50mg
Price
$1540
Updated
2021/12/16
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Nemorexant Chemical Properties,Usage,Production

Uses

[(2S)-2-(6-Chloro-7-methyl-1H-benzimidazol-2-yl)-2-methyl-1-pyrrolidinyl][5-methoxy-2-(2H-1,2,3-triazol-2-yl)phenyl]methanone,

Synthesis

Actelion has applied for a patented synthesis of daridorexant. Starting from the raw amino acid 13.1, it was protected by N-Boc with a yield of 80% (Figure 3.4). Next, amide 13.4 was obtained by HATU-mediated amide coupling with o-phenylenediamine 13.3, which was used directly as a crude product in subsequent reactions. Condensation in hot acetic acid gave benzimidazole 13.5 with a yield of 81%. Removal of the N-Boc protecting group with anhydrous dioxane-hydrochloric acid gave pyrrolidine 13.6; however, the salt equivalent and yield of this step were not reported. Carboxylic acid 13.7 was prepared from the corresponding aryl iodide and 1,2,3-triazole by copper-mediated C-N bond coupling, which finally formed an amide bond with pyrrolidine 13.6 to generate daridorexant (13).

Nemorexant Preparation Products And Raw materials

Raw materials

Preparation Products

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Nemorexant Suppliers

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View Lastest Price from Nemorexant manufacturers

Moxin Chemicals
Product
Daridorexant 1505484-82-1
Price
US $0.00-0.00/mg
Min. Order
10mg
Purity
99%+ HPLC
Supply Ability
1000
Release date
2025-06-27

1505484-82-1, NemorexantRelated Search:


  • Nemorexant
  • Methanone, [(2S)-2-(6-chloro-7-methyl-1H-benzimidazol-2-yl)-2-methyl-1-pyrrolidinyl][5-methoxy-2-(2H-1,2,3-triazol-2-yl)phenyl]-
  • Daridorexant
  • Daridorexant,Nemorexant
  • (S)-[2-(6-Chloro-7-methyl-2-benzimidazolyl)-2-methyl-1-pyrrolidinyl][5-methoxy-2-(2H-1,2,3-triazol-2-yl)phenyl]methanone
  • (S)-(2-(6-chloro-7-methyl-1H-benzo[d]imidazol-2-yl)-2-methylpyrrolidin-1-yl)(5-methoxy-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone
  • emorexant, Daridorexant
  • (2S)-2-(6-Chloro-7-methyl-1H-benzimidazol-2-yl)-2-methyl-1-pyrrolidinyl][5-methoxy-2-(2H-1,2,3-triazol-2-yl)phenyl]methanone
  • 1505484-82-1
  • APIs
  • API