115473-15-9

  • Product Name:Prasugrel
  • Molecular Formula:C7H10ClNOS
  • Molecular Weight:191.681
  • Appearance:Cream solid
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Product Details

pd_meltingpoint:210 °C

Appearance:Cream solid

Purity:99%

Manufacturer Supply Best Quality Prasugrel 115473-15-9 with Efficient Transportation

  • Molecular Formula:C7H10ClNOS
  • Molecular Weight:191.681
  • Appearance/Colour:Cream solid 
  • Melting Point:210 °C 
  • Boiling Point:364.3 °C at 760 mmHg 
  • Flash Point:174.1 °C 
  • PSA:54.40000 
  • LogP:1.67890 

Prasugrel(Cas 115473-15-9) Usage

InChI:InChI=1/C7H9NOS.ClH/c9-7-3-5-4-8-2-1-6(5)10-7;/h3,6,8H,1-2,4H2;1H

115473-15-9 Relevant articles

PROCESS FOR THE PREPARATION OF HIGH-PURITY PRASUGREL

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Page/Page column 13, (2018/04/11)

The field of invention relates to a nove...

A method for preparing prasugrel intermediate

-

Paragraph 0042; 0043, (2018/04/01)

The invention provides a preparation met...

Synthesis of Biologically Active Piperidine Metabolites of Clopidogrel: Determination of Structure and Analyte Development

Shaw, Scott A.,Balasubramanian, Balu,Bonacorsi, Samuel,Cortes, Janet Caceres,Cao, Kevin,Chen, Bang-Chi,Dai, Jun,Decicco, Carl,Goswami, Animesh,Guo, Zhiwei,Hanson, Ronald,Humphreys, W. Griffith,Lam, Patrick Y. S.,Li, Wenying,Mathur, Arvind,Maxwell, Brad D.,Michaudel, Quentin,Peng, Li,Pudzianowski, Andrew,Qiu, Feng,Su, Shun,Sun, Dawn,Tymiak, Adrienne A.,Vokits, Benjamin P.,Wang, Bei,Wexler, Ruth,Wu, Dauh-Rurng,Zhang, Yingru,Zhao, Rulin,Baran, Phil S.

, p. 7019 - 7032 (2015/07/27)

Clopidogrel is a prodrug anticoagulant w...

AN IMPROVED PROCESS FOR THE PREPARATION OF PRASUGREL HYDROCHLORIDE AND ITS INTERMEDIATES

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Page/Page column 20, (2012/01/14)

The present invention provides an improv...

115473-15-9 Process route

5-triphenylmethyl-2-oxo-2,4,5,6,7,7a-hexahydrothieno[3,2-c]pyridine
109904-26-9

5-triphenylmethyl-2-oxo-2,4,5,6,7,7a-hexahydrothieno[3,2-c]pyridine

5,6,7,7a-tetrahydro-thieno[3,2-c]pyridin-2(4H)-one hydrochloride
115473-15-9

5,6,7,7a-tetrahydro-thieno[3,2-c]pyridin-2(4H)-one hydrochloride

Conditions
Conditions Yield
With hydrogenchloride; In water; acetone; at 25 - 50 ℃; for 1h;
99%
With hydrogenchloride; In ethanol; at 45 ℃; Solvent; Inert atmosphere;
76%
With hydrogenchloride; water; In acetone; at 56 ℃; for 3h;
With hydrogenchloride; water; In acetone; at 25 - 30 ℃; for 3h;
With hydrogenchloride; In acetone;
With hydrogenchloride; In water; acetone; at 55 - 60 ℃; for 3h;
With hydrogenchloride; In acetone; at 25 - 30 ℃; for 4.5h; Reflux;
N-trityl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine
109904-25-8

N-trityl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine

5,6,7,7a-tetrahydro-thieno[3,2-c]pyridin-2(4H)-one hydrochloride
115473-15-9

5,6,7,7a-tetrahydro-thieno[3,2-c]pyridin-2(4H)-one hydrochloride

Conditions
Conditions Yield
N-trityl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine; With N,N,N,N,-tetramethylethylenediamine; n-hexyllithium; In toluene; at 0 ℃; Large scale;
With boric acid tributyl ester; In toluene; at 0 ℃; for 1h; Further stages; Large scale;
86.1%
Multi-step reaction with 2 steps
1.1: n-butyllithium / tetrahydrofuran / 1 h / 0 - 15 °C / Inert atmosphere
1.2: 1 h / 0 - 15 °C / Inert atmosphere
1.3: 2 h / 0 - 30 °C
2.1: hydrogenchloride; water / acetone / 3 h / 25 - 30 °C
With hydrogenchloride; n-butyllithium; water; In tetrahydrofuran; acetone;
Multi-step reaction with 2 steps
1.1: n-butyllithium / toluene; hexane; tetrahydrofuran / -5 - 10 °C
1.2: -5 - 10 °C
2.1: hydrogenchloride / water; acetone / 1 h / 25 - 50 °C
With hydrogenchloride; n-butyllithium; In tetrahydrofuran; hexane; water; acetone; toluene;
Multi-step reaction with 2 steps
1.1: n-butyllithium / tetrahydrofuran / 1 h / 0 - 15 °C / Inert atmosphere
1.2: 1 h / 0 - 15 °C
1.3: 1.75 h / 0 - 30 °C / Reflux
2.1: hydrogenchloride / acetone / 4.5 h / 25 - 30 °C / Reflux
With hydrogenchloride; n-butyllithium; In tetrahydrofuran; acetone;

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