1050477-31-0

  • Product Name:Finerenone
  • Molecular Formula:C21H22N4O3
  • Purity:99%
  • Molecular Weight:378.431
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Product Details

  • CasNo: 1050477-31-0
  • Molecular Formula: C21H22N4O3
  • Chinese Manufacturer Supply Finerenone 1050477-31-0 On Stock with Competitive Price

    • Molecular Formula:C21H22N4O3
    • Molecular Weight:378.431
    • Boiling Point:554.7±50.0 °C(Predicted) 
    • PKA:14.76±0.40(Predicted) 
    • PSA:111.25000 
    • Density:1.29±0.1 g/cm3(Predicted) 
    • LogP:4.27338 

    1050477-31-0 Relevant articles

    Synthetic method of fenerenone and intermediate thereof

    -

    Paragraph 0037-0039, (2022/04/06)

    The invention provides a novel synthetic...

    METHOD FOR THE PREPARATION OF (4S)-4-(4-CYANO-2-METHOXYPHENYL)-5-ETHOXY-2,8-DIMETHYL-1,4-DIHYDRO-1-6-NAPHTHYRIDINE-3-CARBOX-AMIDE BY RACEMATE SEPARATION BY MEANS OF DIASTEREOMERIC TARTARIC ACID ESTERS

    -

    Paragraph 0151; 0162-0169; 0174; 0176-0182; 0191-0247, (2021/06/04)

    The present invention relates to a novel...

    PROCESS FOR PREPARING (4S)-4-(4-CYANO-2-METHOXYPHENYL)-5-ETHOXY-2,8-DIMETHYL-1,4-DIHYDRO-1,6-NAPHTHYRIDINE-3-CARBOXAMIDE ENABLED BY A CATALYTIC ASYMMETRIC HANTZSCH ESTER REDUCTION

    -

    , (2022/01/06)

    The present invention relates to a novel...

    Enantioselective Total Synthesis of (?)-Finerenone Using Asymmetric Transfer Hydrogenation

    Aggarwal, Varinder K.,Farrar, Elliot H. E.,Gandhamsetty, Narasimhulu,Grayson, Matthew N.,Lerchen, Andreas,Platzek, Johannes,Winter, Nils

    supporting information, p. 23107 - 23111 (2020/12/01)

    (?)-Finerenone is a nonsteroidal mineral...

    1050477-31-0 Process route

    finerenone (+)O,O-dibenzoyl-D-tartaric acid

    finerenone (+)O,O-dibenzoyl-D-tartaric acid

    BAY<sub>948862</sub>
    1050477-31-0

    BAY948862

    Conditions
    Conditions Yield
    With sodium phosphate; In ethanol; water; toluene; at 23 - 50 ℃; for 6h; pH=4 - 7.5; Temperature; pH-value;
    97.07%
    rac-4-(4-cyano-2-methoxyphenyl)-5-ethoxy-2,8-dimethyl-1,6-naphthyridine-3-carboxamide

    rac-4-(4-cyano-2-methoxyphenyl)-5-ethoxy-2,8-dimethyl-1,6-naphthyridine-3-carboxamide

    BAY<sub>948862</sub>
    1050477-31-0

    BAY948862

    Conditions
    Conditions Yield
    With (R)-3,3'-bis(9-anthracenyl)-1,1'-binaphthyl-2,2'-diyl hydrogenphosphate; diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate; In tetrahydrofuran; at 40 - 100 ℃; for 24h; enantioselective reaction; Inert atmosphere;
    82%
    Multi-step reaction with 2 steps
    1: N,N,N,N-tetraethylammonium tetrafluoroborate / methanol / 4.5 h / Electrochemical reaction
    2: Chiralpak AS-V, 20 μm. / methanol; acetonitrile / 22502.3 Torr / Resolution of racemate; Large scale
    With N,N,N,N-tetraethylammonium tetrafluoroborate; In methanol; acetonitrile;
    Multi-step reaction with 4 steps
    1: N,N,N,N-tetraethylammonium tetrafluoroborate / methanol / 4.5 h / Electrochemical reaction
    2: Chiralpak AS-V, 20 μm. / methanol; acetonitrile / 22502.3 Torr / Resolution of racemate; Large scale
    3: nitric acid / acetonitrile / 9.5 h / 9 - 20 °C / Inert atmosphere
    4: N,N,N,N-tetraethylammonium tetrafluoroborate / methanol / 5 h / Electrochemical reaction
    With nitric acid; N,N,N,N-tetraethylammonium tetrafluoroborate; In methanol; acetonitrile;
    Multi-step reaction with 4 steps
    1: N,N,N,N-tetraethylammonium tetrafluoroborate / methanol / 4.5 h / Electrochemical reaction
    2: Chiralpak AS-V, 20 μm. / methanol; acetonitrile / 22502.3 Torr / Resolution of racemate; Large scale
    3: nitric acid / acetonitrile / 9.5 h / 9 - 20 °C / Inert atmosphere
    4: N,N,N,N-tetraethylammonium tetrafluoroborate / methanol / 6 h / Electrochemical reaction
    With nitric acid; N,N,N,N-tetraethylammonium tetrafluoroborate; In methanol; acetonitrile;
    Multi-step reaction with 4 steps
    1: N,N,N,N-tetraethylammonium tetrafluoroborate / methanol / 4.5 h / Electrochemical reaction
    2: Chiralpak AS-V, 20 μm. / methanol; acetonitrile / 22502.3 Torr / Resolution of racemate; Large scale
    3: 2,3-dicyano-5,6-dichloro-p-benzoquinone / dichloromethane / 1 h / 20 °C
    4: N,N,N,N-tetraethylammonium tetrafluoroborate / methanol / 5 h / Electrochemical reaction
    With N,N,N,N-tetraethylammonium tetrafluoroborate; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In methanol; dichloromethane; acetonitrile;

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