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(R)-Zopiclone

Base Information Edit
  • Chemical Name:(R)-Zopiclone
  • CAS No.:138680-08-7
  • Molecular Formula:C17H17ClN6O3
  • Molecular Weight:388.813
  • Hs Code.:2933790002
  • UNII:7A997Q53NR
  • DSSTox Substance ID:DTXSID40160758
  • Nikkaji Number:J573.433I
  • Wikidata:Q27124198
  • Metabolomics Workbench ID:58744
  • ChEMBL ID:CHEMBL250053
  • Mol file:138680-08-7.mol
(R)-Zopiclone

Synonyms:(R)-Zopiclone;Zopiclone, (R)-;138680-08-7;(-)-Zopiclone;(5R)-zopiclone;UNII-7A997Q53NR;Zopiclone R-isomer RS [USP];7A997Q53NR;CHEBI:53762;(-)-(5R)-6-(5-Chloropyridin-2-yl)-7-oxo-6,7-dihydro-5H-pyrrolo(3,4-b)pyrazin-5-yl 4-methylpiperazine-1-carboxylate;(5R)-6-(5-chloropyridin-2-yl)-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-5-yl 4-methylpiperazine-1-carboxylate;[(7R)-6-(5-chloropyridin-2-yl)-5-oxo-7H-pyrrolo[3,4-b]pyrazin-7-yl] 4-methylpiperazine-1-carboxylate;1-Piperazinecarboxylic acid, 4-methyl-, (5R)-6-(5-chloro-2-pyridinyl)-6,7-dihydro-7-oxo-5H-pyrrolo(3,4-b)pyrazin-5-yl ester;(R)-zolpiclone;ZPC;Tocris-1094;Lopac-Z-4900;CHEMBL250053;SCHEMBL2779919;DTXSID40160758;NCGC00016108-01;NCGC00016108-02;NCGC00016108-03;NCGC00016108-07;NCGC00016108-08;NCGC00024993-01;ZOPICLONE R-ISOMER [USP IMPURITY];Q27124198;(6-(5-Chloro-2-pyridyl)-6,7-dihydro-7-oxo-5H-pyrrolo (3,4-b)pyrazin-5-yl)-4-methyl-1-piperazine carboxylate

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Chemical Property of (R)-Zopiclone Edit
Chemical Property:
  • Boiling Point:580.7±50.0 °C(Predicted) 
  • PKA:6.70±0.10(Predicted) 
  • PSA:91.76000 
  • Density:1.54±0.1 g/cm3(Predicted) 
  • LogP:1.50880 
  • XLogP3:0.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:7
  • Rotatable Bond Count:3
  • Exact Mass:388.1050661
  • Heavy Atom Count:27
  • Complexity:573
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CN1CCN(CC1)C(=O)OC2C3=NC=CN=C3C(=O)N2C4=NC=C(C=C4)Cl
  • Isomeric SMILES:CN1CCN(CC1)C(=O)O[C@@H]2C3=NC=CN=C3C(=O)N2C4=NC=C(C=C4)Cl
  • Uses (R)-Zopiclone is the (R)-enantiomer of Zopiclone (Z700500). (R)-Zopiclone is known to have sedative and anxiolytic effects and as well as effects towards locomotor activity reduction.
Technology Process of (R)-Zopiclone

There total 9 articles about (R)-Zopiclone 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:
Guidance literature:
With potassium carbonate; In dichloromethane; water; at 20 ℃; pH=10;
Guidance literature:
With potassium carbonate; In dichloromethane; water; ethyl acetate; at 30 - 65 ℃;