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(8S)-N,N,2,3-Tetramethyl-8-(2-methylphenyl)-3,6,7,8-tetrahydropyrano[2,3-e]benzimidazole-5-carboxamide

Base Information
  • Chemical Name:(8S)-N,N,2,3-Tetramethyl-8-(2-methylphenyl)-3,6,7,8-tetrahydropyrano[2,3-e]benzimidazole-5-carboxamide
  • CAS No.:917957-11-0
  • Molecular Formula:C22H25N3O2
  • Molecular Weight:363.459
  • Hs Code.:
  • ChEMBL ID:CHEMBL1098860
  • DSSTox Substance ID:DTXSID50575551
  • Nikkaji Number:J2.641.111D
(8S)-N,N,2,3-Tetramethyl-8-(2-methylphenyl)-3,6,7,8-tetrahydropyrano[2,3-e]benzimidazole-5-carboxamide

Synonyms:BYK-405879;917957-11-0;SCHEMBL2689406;CHEMBL1098860;DTXSID50575551;(8S)-N,N,2,3-Tetramethyl-8-(2-methylphenyl)-3,6,7,8-tetrahydropyrano[2,3-e]benzimidazole-5-carboxamide

Suppliers and Price of (8S)-N,N,2,3-Tetramethyl-8-(2-methylphenyl)-3,6,7,8-tetrahydropyrano[2,3-e]benzimidazole-5-carboxamide
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (8S)-N,N,2,3-Tetramethyl-8-(2-methylphenyl)-3,6,7,8-tetrahydropyrano[2,3-e]benzimidazole-5-carboxamide
Chemical Property:
  • XLogP3:3.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:2
  • Exact Mass:363.19467705
  • Heavy Atom Count:27
  • Complexity:554
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=CC=CC=C1C2CCC3=C(O2)C4=C(C=C3C(=O)N(C)C)N(C(=N4)C)C
  • Isomeric SMILES:CC1=CC=CC=C1[C@@H]2CCC3=C(O2)C4=C(C=C3C(=O)N(C)C)N(C(=N4)C)C
Technology Process of (8S)-N,N,2,3-Tetramethyl-8-(2-methylphenyl)-3,6,7,8-tetrahydropyrano[2,3-e]benzimidazole-5-carboxamide

There total 3 articles about (8S)-N,N,2,3-Tetramethyl-8-(2-methylphenyl)-3,6,7,8-tetrahydropyrano[2,3-e]benzimidazole-5-carboxamide 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 ammonium hydroxide; In dichloromethane; for 0.5h;
DOI:10.1021/op800177x
Guidance literature:
With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 20 ℃; for 0.25 - 16.75h; Product distribution / selectivity;
Guidance literature:
4-hydroxy-N,N,1,2-tetramethyl-5-[3-(2-methylphenyl)-3-oxopropyl]-1H-benzimidazole-6-carboxamide; With potassium tert-butylate; hydrogen; RuCl2[(S)-Xyl-P-Phos][(S)-DAIPEN]; In isopropyl alcohol; tert-butyl alcohol; at 70 ℃; for 20h; under 60006 Torr;
With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 20 ℃; for 0.25h; Further stages. Title compound not separated from byproducts.;
DOI:10.1016/j.tetasy.2008.08.022
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