1321514-06-0

  • Product Name:AZD-4635
  • Molecular Weight:315.737
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Product Details

Purity:99%

Quality manufacturer supply AZD-4635 1321514-06-0 in stock with high standard

  • Molecular Formula:C15H11ClFN5
  • Molecular Weight:315.737
  • Boiling Point:491.5±55.0 °C(Predicted) 
  • PKA:1.75±0.63(Predicted) 
  • Density:1.387±0.06 g/cm3(Predicted) 

1321514-06-0 Relevant articles

Synthetic Route Design of AZD4635, an A2AR Antagonist

Littleson, Mairi M.,Campbell, Andrew D.,Clarke, Adam,Dow, Mark,Ensor, Gareth,Evans, Matthew C.,Herring, Adam,Jackson, Bethany A.,Jackson, Lucinda V.,Karlsson, Staffan,Klauber, David J.,Legg, Danny H.,Leslie, Kevin W.,Morav?ík, ?tefan,Parsons, Chris D.,Ronson, Thomas O.,Meadows, Rebecca E.

, p. 1407 - 1419 (2019)

The AstraZeneca approach to synthetic Ro...

Multikilogram-Scale Preparation of AZD4635 via C-H Borylation and Bromination: The Corrosion of Tantalum by a Bromine/Methanol Mixture

Douglas, James J.,Adams, Bradley W. V.,Benson, Helen,Broberg, Karl,Gillespie, Paul M.,Hoult, Oliver,Ibraheem, Ameer K.,Janbon, Sophie,Janin, Guillaume,Parsons, Chris D.,Sigerson, Ralph C.,Klauber, David J.

supporting information, p. 62 - 68 (2019/01/15)

An efficient route to AZD4635 has been d...

1,2,4-TRIAZINE-4-AMINE DERIVATIVES

-

Page/Page column 177, (2011/09/14)

According to the invention there is prov...

1321514-06-0 Process route

2-chloro-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
697739-22-3

2-chloro-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

6-bromo-5-(4-fluorophenyl)-1,2,4-triazin-3-amine
1321517-59-2

6-bromo-5-(4-fluorophenyl)-1,2,4-triazin-3-amine

6-(2-chloro-6-methylpyridin-4-yl)-5-(4-fluorophenyl)-1,2,4-triazin-3-amine
1321514-06-0

6-(2-chloro-6-methylpyridin-4-yl)-5-(4-fluorophenyl)-1,2,4-triazin-3-amine

Conditions
Conditions Yield
With (4-(N,N-dimethylamino)phenyl)-di-tert-butylphosphine; palladium diacetate; potassium carbonate; In tetrahydrofuran; water; at 62 - 66 ℃; Inert atmosphere; Large scale;
84.5%
With potassium carbonate; dichloro bis((p-dimethylaminophenyl)-?-di-tert-butylphosphine)palladium(II); In 1,4-dioxane; water; Product distribution / selectivity; Inert atmosphere; Reflux;
61%
2-chloro-4,6-dimethyl-pyridine
30838-93-8

2-chloro-4,6-dimethyl-pyridine

6-(2-chloro-6-methylpyridin-4-yl)-5-(4-fluorophenyl)-1,2,4-triazin-3-amine
1321514-06-0

6-(2-chloro-6-methylpyridin-4-yl)-5-(4-fluorophenyl)-1,2,4-triazin-3-amine

C<sub>15</sub>H<sub>11</sub>ClFN<sub>5</sub>

C15H11ClFN5

Conditions
Conditions Yield
Multi-step reaction with 3 steps
1.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / 0 °C / Inert atmosphere
1.2: 15 h / 20 °C / Inert atmosphere
2.1: trifluoroacetic acid / dichloromethane / 24 h / Inert atmosphere
3.1: zinc trifluoromethanesulfonate / isopropyl alcohol / 24 h / 50 °C
With zinc trifluoromethanesulfonate; trifluoroacetic acid; lithium hexamethyldisilazane; In tetrahydrofuran; dichloromethane; isopropyl alcohol;
Multi-step reaction with 3 steps
1: lithium hexamethyldisilazane / tetrahydrofuran / 10 °C / Inert atmosphere
2: toluene-4-sulfonic acid; N-chloro-succinimide / water; dichloromethane / 2 h / Inert atmosphere
3: sodium iodide / ethanol / 20 - 75 °C / Inert atmosphere
With N-chloro-succinimide; toluene-4-sulfonic acid; sodium iodide; lithium hexamethyldisilazane; In tetrahydrofuran; ethanol; dichloromethane; water;
Multi-step reaction with 3 steps
1: lithium hexamethyldisilazane / tetrahydrofuran / 10 °C / Inert atmosphere
2: copper(II) acetate monohydrate; potassium carbonate; 2,3-dimethyl-2,3-diaminobutane / acetonitrile / 72 h
3: zinc trifluoromethanesulfonate / isopropyl alcohol / 24 h / 50 °C
With 2,3-dimethyl-2,3-diaminobutane; copper(II) acetate monohydrate; zinc trifluoromethanesulfonate; potassium carbonate; lithium hexamethyldisilazane; In tetrahydrofuran; isopropyl alcohol; acetonitrile;
Multi-step reaction with 3 steps
1: lithium hexamethyldisilazane / 2-methyltetrahydrofuran / 20 °C / Inert atmosphere
2: toluene-4-sulfonic acid; N-chloro-succinimide / water; dichloromethane / 2 h / Inert atmosphere
3: sodium iodide / ethanol / 20 - 75 °C / Inert atmosphere
With N-chloro-succinimide; toluene-4-sulfonic acid; sodium iodide; lithium hexamethyldisilazane; In 2-methyltetrahydrofuran; ethanol; dichloromethane; water;
Multi-step reaction with 3 steps
1: lithium hexamethyldisilazane / 2-methyltetrahydrofuran / 20 °C / Inert atmosphere
2: copper(II) acetate monohydrate; potassium carbonate; 2,3-dimethyl-2,3-diaminobutane / acetonitrile / 72 h
3: zinc trifluoromethanesulfonate / isopropyl alcohol / 24 h / 50 °C
With 2,3-dimethyl-2,3-diaminobutane; copper(II) acetate monohydrate; zinc trifluoromethanesulfonate; potassium carbonate; lithium hexamethyldisilazane; In 2-methyltetrahydrofuran; isopropyl alcohol; acetonitrile;

1321514-06-0 Upstream products

  • 697739-22-3
    697739-22-3

    2-chloro-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

  • 1321517-59-2
    1321517-59-2

    6-bromo-5-(4-fluorophenyl)-1,2,4-triazin-3-amine

  • 107128-47-2
    107128-47-2

    5-(4-fluorophenyl)-1,2,4-triazin-3-amine

  • 447-43-8
    447-43-8

    1-(4-fluorophenyl)-2,2-dihydroxyethan-1-one

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