1005450-55-4

  • Product Name:N-((R)-1-(naphthalen-1-yl)ethyl)-3-(3-(trifluoroMethyl)phenyl)propanaMide
  • Molecular Formula:C22H20F3NO
  • Purity:99%
  • Molecular Weight:371.402
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Product Details

Reputable Manufacturer Supply High Purity N-((R)-1-(naphthalen-1-yl)ethyl)-3-(3-(trifluoroMethyl)phenyl)propanaMide 1005450-55-4 with Efficient Shipping

  • Molecular Formula:C22H20F3NO
  • Molecular Weight:371.402
  • Melting Point:90-92℃ (cyclohexane ) 
  • Boiling Point:530.5±50.0 °C(Predicted) 
  • PKA:15.18±0.46(Predicted) 
  • PSA:29.10000 
  • Density:1.210±0.06 g/cm3(Predicted) 
  • LogP:6.05950 

1005450-55-4 Relevant articles

Practical synthesis of the calcimimetic agent, cinacalcet

Thiel, Oliver R.,Bernard, Charles,Tormos, Wanda,Brewin, Alan,Hirotani, Shuji,Murakami, Kazuo,Saito, Kenji,Larsen, Robert D.,Martinelli, Michael J.,Reider, Paul J.

, p. 13 - 15 (2008)

A practical synthesis of cinacalcet (Sen...

Enantioselective synthesis of (R)-Cinacalcet via cobalt-catalysed asymmetric Negishi cross-coupling

Sun, Xiao,Wang, Xueyang,Liu, Feipeng,Gao, Zidong,Bian, Qinghua,Wang, Min,Zhong, Jiangchun

, p. 682 - 687 (2019)

A novel enantioselective synthesis of (R...

Method for synthesizing cinacalcet intermediate

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Paragraph 0007; 0013-0019, (2020/04/02)

The invention particularly discloses a m...

Preparation method of cinacalcet hydrochloride

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Paragraph 0036; 0038; 0040; 0043-0047, (2020/10/05)

The invention provides a preparation met...

Preparation method of cinacalcet hydrochloride and intermediate thereof

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, (2020/06/09)

The invention discloses a preparation me...

Synthesis method of cinacalcet hydrochloride intermediate

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Paragraph 0061-0068, (2020/05/01)

The invention provides a preparation met...

1005450-55-4 Process route

3-(3-trifluoromethylphenyl)propanoic acid
585-50-2

3-(3-trifluoromethylphenyl)propanoic acid

(R)-<1-(1-Naphthyl)ethyl>ammonium chloride
82572-04-1

(R)-<1-(1-Naphthyl)ethyl>ammonium chloride

(R)‐N‐(1‐(naphthalen‐1‐yl)ethyl)‐3‐(3‐trifluoromethylphenyl)propanamide
1005450-55-4,955371-05-8

(R)‐N‐(1‐(naphthalen‐1‐yl)ethyl)‐3‐(3‐trifluoromethylphenyl)propanamide

Conditions
Conditions Yield
(R)-<1-(1-Naphthyl)ethyl>ammonium chloride; With sodium hydroxide; In toluene;
3-(3-trifluoromethylphenyl)propanoic acid; In toluene; at 140 - 150 ℃; Further stages.;
95%
(R)-N-(1-naphthalen-1-yl-ethyl)-3-(3-trifluoromethyl-phenyl)-(E)-acrylamide
1095393-66-0

(R)-N-(1-naphthalen-1-yl-ethyl)-3-(3-trifluoromethyl-phenyl)-(E)-acrylamide

(R)‐N‐(1‐(naphthalen‐1‐yl)ethyl)‐3‐(3‐trifluoromethylphenyl)propanamide
1005450-55-4,955371-05-8

(R)‐N‐(1‐(naphthalen‐1‐yl)ethyl)‐3‐(3‐trifluoromethylphenyl)propanamide

Conditions
Conditions Yield
With hydrogen; palladium on activated carbon; In methanol; toluene; at 20 ℃; for 1.5h; Product distribution / selectivity;
91.2%
With hydrogen; nickel; In methanol; at 45 - 50 ℃; for 3h; under 3677.86 Torr; Product distribution / selectivity;
 
With hydrogen; palladium on activated charcoal; at 20 ℃; for 3h; under 3677.86 Torr; Product distribution / selectivity;
 

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1005450-55-4 Downstream products

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