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Facinicline hydrochloride

Base Information Edit
  • Chemical Name:Facinicline hydrochloride
  • CAS No.:677305-02-1
  • Molecular Formula:C15H18N4O.ClH
  • Molecular Weight:
  • Hs Code.:
  • UNII:O6J463N18M
  • Wikidata:Q27285409
  • ChEMBL ID:CHEMBL5095032
  • Mol file:677305-02-1.mol
Facinicline hydrochloride

Synonyms:N-((3S)-1-azabicyclo(2.2.2)oct-3-yl)-1H-indazole-3-carboxamide hydrochloride;RG3487

Suppliers and Price of Facinicline hydrochloride
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 3 raw suppliers
Chemical Property of Facinicline hydrochloride Edit
Chemical Property:
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:306.1247389
  • Heavy Atom Count:21
  • Complexity:380
Purity/Quality:

97% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Canonical SMILES:C1CN2CCC1C(C2)NC(=O)C3=NNC4=CC=CC=C43.Cl
  • Isomeric SMILES:C1CN2CCC1[C@@H](C2)NC(=O)C3=NNC4=CC=CC=C43.Cl
  • Recent ClinicalTrials:Study to Evaluate the Safety and Efficacy of MEM 3454 as Adjunctive Treatment in Combination With a Preexisting Antipsychotic in Patients With Cognitive Impairment Associated With Schizophrenia
Technology Process of Facinicline hydrochloride

There total 5 articles about Facinicline hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 53.0%

Guidance literature:
Guidance literature:
(S)-1-azabicyclo[2.2.2]oct-3-ylamine dihydrochloride; 1H-Indazole-3-carboxylic acid; With thionyl chloride; N,N-dimethyl-formamide; In toluene; at 80 ℃; for 4h;
With triethylamine; In N,N-dimethyl-formamide; at 70 ℃; for 4h;
With hydrogenchloride; In methanol; tert-butyl methyl ether; water; at 5 ℃;
Guidance literature:
Multi-step reaction with 5 steps
1.1: water / 3 h / 25 - 30 °C
2.1: dichloromethane / 2 h / 40 °C
3.1: aluminum (III) chloride / dichloromethane / 2 h / 30 °C / Reflux
4.1: hydrogenchloride; acetic acid / water / 1 h / 90 °C
4.2: 0.5 h / 115 °C
5.1: thionyl chloride / N,N-dimethyl-formamide / toluene / 4 h / 80 °C
5.2: 4 h / 70 °C
5.3: 5 °C
With hydrogenchloride; aluminum (III) chloride; thionyl chloride; acetic acid; N,N-dimethyl-formamide; In dichloromethane; water; toluene;
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