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1050477-31-0

  • Product Name:Finerenone
  • Molecular Formula:C21H22N4O3
  • Molecular Weight:378.431
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Product Details

Purity:99%

Chinese factory supply Finerenone 1050477-31-0 in stock with high standard

  • 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

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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

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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

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, (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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