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
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
N-Bromosuccinimide Price
- Product number
- CS-0039396
- Product name
- Nemorexant
- Purity
- 99.56%
- Packaging
- 1mg
- Price
- $100
- Updated
- 2021/12/16
- Product number
- CS-0039396
- Product name
- Nemorexant
- Purity
- 99.56%
- Packaging
- 5mg
- Price
- $320
- Updated
- 2021/12/16
- Product number
- CS-0039396
- Product name
- Nemorexant
- Purity
- 99.56%
- Packaging
- 10mg
- Price
- $530
- Updated
- 2021/12/16
- Product number
- CS-0039396
- Product name
- Nemorexant
- Purity
- 99.56%
- Packaging
- 25mg
- Price
- $1050
- Updated
- 2021/12/16
- Product number
- CS-0039396
- Product name
- Nemorexant
- Purity
- 99.56%
- Packaging
- 50mg
- Price
- $1540
- Updated
- 2021/12/16
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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View Lastest Price from Nemorexant manufacturers
- 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