1632051-40-1

  • Product Name:Zuranolone
  • Molecular Weight:409.572
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Product Details

Purity:99%

Factory Supply industrial standard Zuranolone 1632051-40-1 In Stock

  • Molecular Formula:C25H35N3O2
  • Molecular Weight:409.572
  • Boiling Point:574.3±30.0 °C(Predicted) 
  • PKA:15.17±0.60(Predicted) 
  • Density:1.32±0.1 g/cm3(Predicted) 

1632051-40-1 Relevant articles

FORMULATIONS OF 19-NOR C3,3- DISUBSTITUTED C21-N-PYRAZOLYL STEROID AND METHODS OF USE THEREOF

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Paragraph 00488, (2022/02/05)

This invention relates to a 19-nor C3,3-...

Neuroactive Steroids. 2. 3α-Hydroxy-3β-methyl-21-(4-cyano-1H-pyrazol-1′-yl)-19-nor-5β-pregnan-20-one (SAGE-217): A Clinical Next Generation Neuroactive Steroid Positive Allosteric Modulator of the (γ-Aminobutyric Acid)A Receptor

Martinez Botella, Gabriel,Salituro, Francesco G.,Harrison, Boyd L.,Beresis, Richard T.,Bai, Zhu,Blanco, Maria-Jesus,Belfort, Gabriel M.,Dai, Jing,Loya, Carlos M.,Ackley, Michael A.,Althaus, Alison L.,Grossman, Scott J.,Hoffmann, Ethan,Doherty, James J.,Robichaud, Albert J.

, p. 7810 - 7819 (2017/10/06)

Certain classes of neuroactive steroids ...

19-NOR C3,3-DISUBSTITUTED C21-N-PYRAZOLYL STEROIDS AND METHODS OF USE THEREOF

-

, (2014/11/11)

Provided herein are 19-nor C3,3-disubsti...

1632051-40-1 Process route

2-bromo-1-((3R,5R,8R,9R,10S,13S,14S,17S)-3-hydroxy-3,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)ethan-1-one
1430063-93-6

2-bromo-1-((3R,5R,8R,9R,10S,13S,14S,17S)-3-hydroxy-3,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)ethan-1-one

1H-pyrazole-4-carbonitrile
31108-57-3

1H-pyrazole-4-carbonitrile

zuranolone
1632051-40-1

zuranolone

Conditions
Conditions Yield
With potassium carbonate; In tetrahydrofuran; at 20 ℃; for 15h;
17.4%
With potassium carbonate; In tetrahydrofuran; at 20 ℃; for 15h;
17.4%
With potassium carbonate; In tetrahydrofuran; at 20 ℃; for 15h;
17.4%
With potassium carbonate; In tetrahydrofuran;
28 g
(3R,5R,8R,9R,10S,13S,14S)-3-hydroxy-3,13-dimethyl-1,2,4,5,6,7,8,9,10,1 1,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one

(3R,5R,8R,9R,10S,13S,14S)-3-hydroxy-3,13-dimethyl-1,2,4,5,6,7,8,9,10,1 1,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one

zuranolone
1632051-40-1

zuranolone

Conditions
Conditions Yield
Multi-step reaction with 5 steps
1.1: potassium tert-butylate / tetrahydrofuran / 1 h / 0 - 60 °C
1.2: 18 h / 60 °C
2.1: dimethylsulfide borane complex / tetrahydrofuran / 14 - 20 °C / Cooling with ice
2.2: 2 h / 14 - 20 °C
3.1: pyridinium chlorochromate / dichloromethane / 3 h / 0 - 22 °C
4.1: bromine; hydrogen bromide / water; methanol / 1.5 h / 17 °C
5.1: potassium carbonate / tetrahydrofuran / 15 h / 20 °C
With dimethylsulfide borane complex; potassium tert-butylate; hydrogen bromide; bromine; potassium carbonate; pyridinium chlorochromate; In tetrahydrofuran; methanol; dichloromethane; water;
Multi-step reaction with 5 steps
1: potassium tert-butylate / tetrahydrofuran
2: borane / tetrahydrofuran
3: pyridinium chlorochromate / dichloromethane
4: bromine; hydrogen bromide / water; methanol
5: potassium carbonate / tetrahydrofuran
With borane; potassium tert-butylate; hydrogen bromide; bromine; potassium carbonate; pyridinium chlorochromate; In tetrahydrofuran; methanol; dichloromethane; water;

1632051-40-1 Upstream products

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  • 1430063-93-6
    1430063-93-6

    2-bromo-1-((3R,5R,8R,9R,10S,13S,14S,17S)-3-hydroxy-3,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-17-yl)ethan-1-one

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    1H-pyrazole-4-carbonitrile

  • 1430063-92-5
    1430063-92-5

    (3R,5R,8R,9R,10S,13S,14S,17S)-17-(1-hydroxyethyl)-3,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthren-3-ol

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