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NMS-P715

Base Information Edit
  • Chemical Name:NMS-P715
  • CAS No.:1202055-34-2
  • Molecular Formula:C35H39F3N8O3
  • Molecular Weight:676.7311696
  • Hs Code.:
  • Mol file:1202055-34-2.mol
NMS-P715

Synonyms:NMS-P715;N-(2,6-diethylphenyl)-1-Methyl-8-({4-[(1-Methylpiperidin-4-yl)carbaMoyl]-2-(trifluoroMethoxy)phenyl}aMino)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxaMide;NMS P715 analog;NMS-P 715 analog;NMS-P715 analog;N-(2,6-diethylphenyl)-1-methyl-8-((4-((1-methylpiperidin-4-yl)carbamoyl)-2-(trifluoromethoxy)phenyl)amino)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide NMS-P715

Suppliers and Price of NMS-P715
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
  • Crysdot
  • NMS-P715analog 98+%
  • 5mg
  • $ 111.00
  • American Custom Chemicals Corporation
  • NMS-P715 95.00%
  • 5MG
  • $ 358.60
Total 11 raw suppliers
Chemical Property of NMS-P715 Edit
Chemical Property:
  • PKA:11.75±0.70(Predicted) 
  • PSA:126.30000 
  • Density:1.32±0.1 g/cm3(Predicted) 
  • LogP:5.40380 
Purity/Quality:

98%min *data from raw suppliers

NMS-P715analog 98+% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of NMS-P715

There total 9 articles about NMS-P715 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:
Multi-step reaction with 5 steps
1: water; potassium hydroxide / ethanol / 1 h / Reflux
2: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C
3: tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; XPhos / 1,4-dioxane / 8 h / 90 °C / Inert atmosphere
4: trifluoroacetic acid / N,N-dimethyl-formamide / 20 °C
5: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 24 h / 20 °C
With tris-(dibenzylideneacetone)dipalladium(0); water; benzotriazol-1-ol; caesium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; potassium hydroxide; XPhos; In 1,4-dioxane; ethanol; N,N-dimethyl-formamide; 3: Buchwald-Hartwig coupling;
DOI:10.1016/j.bmcl.2011.05.122
Guidance literature:
Multi-step reaction with 4 steps
1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C
2: tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; XPhos / 1,4-dioxane / 8 h / 90 °C / Inert atmosphere
3: trifluoroacetic acid / N,N-dimethyl-formamide / 20 °C
4: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 24 h / 20 °C
With tris-(dibenzylideneacetone)dipalladium(0); benzotriazol-1-ol; caesium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; XPhos; In 1,4-dioxane; N,N-dimethyl-formamide; 2: Buchwald-Hartwig coupling;
DOI:10.1016/j.bmcl.2011.05.122
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