2239273-34-6

  • Product Name:AB-928
  • Molecular Weight:426.481
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Product Details

Purity:99%

Reputable manufacturer supply AB-928 2239273-34-6 in stock with high standard

  • Molecular Formula:C23H22N8O
  • Molecular Weight:426.481

2239273-34-6 Relevant articles

Development of a Scalable and Practical Synthesis of AB928, a Dual A2a/A2bReceptor Antagonist

Debien, Laurent P. P.,Jeffrey, Jenna L.,Leleti, Manmohan R.,Miles, Dillon H.,Powers, Jay P.,Rosen, Brandon R.,Sharif, Ehesan U.

, p. 1254 - 1261 (2020/08/14)

AB928 is a potent and selective dual ant...

SOLID FORMS OF AN AZOLOPYRIMIDINE COMPOUND

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Paragraph 0207; 0213, (2020/02/14)

The present invention provides solid for...

PROCESSES FOR PREPARING AMINOPYRIMIDINE COMPOUNDS

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Paragraph 0078, (2020/12/29)

Provided herein are improved processes f...

DOSING WITH AN AZOLOPYRIMIDINE COMPOUND

-

, (2019/09/04)

Provided herein are methods of treating ...

2239273-34-6 Process route

2-(6-(azidomethyl)pyridin-2-yl)propan-2-ol
1202403-01-7

2-(6-(azidomethyl)pyridin-2-yl)propan-2-ol

3-(2-amino-6-ethynylpyrimidin-4-yl)-2-methylbenzonitrile

3-(2-amino-6-ethynylpyrimidin-4-yl)-2-methylbenzonitrile

3-(2-amino-6-(1-((6-(2-hydroxypropan-2-yl)pyridin-2-yl)methyl)-1H-1,2,3-triazol-4-yl)pyrimidin-4-yl)-2-methylbenzonitrile
2239273-34-6

3-(2-amino-6-(1-((6-(2-hydroxypropan-2-yl)pyridin-2-yl)methyl)-1H-1,2,3-triazol-4-yl)pyrimidin-4-yl)-2-methylbenzonitrile

Conditions
Conditions Yield
With copper(ll) sulfate pentahydrate; sodium L-ascorbate; In water; tert-butyl alcohol; at 60 ℃; for 13h;
90%
With copper(II) sulfate; sodium L-ascorbate; In water; tert-butyl alcohol; at 60 ℃; for 13h;
90%
With copper(ll) sulfate pentahydrate; sodium L-ascorbate; In water; tert-butyl alcohol; at 60 ℃; for 13h;
90%
With copper(ll) sulfate pentahydrate; sodium L-ascorbate;
90%
With copper(I) sulfate pentahydrate; sodium L-ascorbate; In tetrahydrofuran; tert-butyl methyl ether; water; at 60 ℃; for 20h; Solvent; Temperature;
3-(2-amino-6-{2-[tris(propan-2-yl)silyl]ethynyl}-pyrimidin-4-yl)-2-methylbenzonitrile

3-(2-amino-6-{2-[tris(propan-2-yl)silyl]ethynyl}-pyrimidin-4-yl)-2-methylbenzonitrile

3-(2-amino-6-(1-((6-(2-hydroxypropan-2-yl)pyridin-2-yl)methyl)-1H-1,2,3-triazol-4-yl)pyrimidin-4-yl)-2-methylbenzonitrile
2239273-34-6

3-(2-amino-6-(1-((6-(2-hydroxypropan-2-yl)pyridin-2-yl)methyl)-1H-1,2,3-triazol-4-yl)pyrimidin-4-yl)-2-methylbenzonitrile

Conditions
Conditions Yield
Multi-step reaction with 2 steps
1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.25 h / 0 °C
2: copper(ll) sulfate pentahydrate; sodium L-ascorbate / water; tert-butyl alcohol / 13 h / 60 °C
With copper(ll) sulfate pentahydrate; tetrabutyl ammonium fluoride; sodium L-ascorbate; In tetrahydrofuran; water; tert-butyl alcohol;
Multi-step reaction with 2 steps
1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.25 h / 0 °C
2: copper(II) sulfate; sodium L-ascorbate / water; tert-butyl alcohol / 13 h / 60 °C
With tetrabutyl ammonium fluoride; copper(II) sulfate; sodium L-ascorbate; In tetrahydrofuran; water; tert-butyl alcohol;
Multi-step reaction with 2 steps
1: tetra(n-butyl)ammonium hydroxide / tetrahydrofuran / 0.5 h / 0 - 20 °C
2: sodium L-ascorbate; copper(I) sulfate pentahydrate / water; tetrahydrofuran; tert-butyl methyl ether / 20 h / 60 °C
With copper(I) sulfate pentahydrate; tetra(n-butyl)ammonium hydroxide; sodium L-ascorbate; In tetrahydrofuran; tert-butyl methyl ether; water;
Multi-step reaction with 2 steps
1: dipotassium hydrogenphosphate; tetra(n-butyl)ammonium hydroxide / water; tetrahydrofuran / 1.5 h / 20 °C
2: sodium L-ascorbate; copper(I) sulfate pentahydrate / water; tetrahydrofuran; tert-butyl methyl ether / 20 h / 60 °C
With dipotassium hydrogenphosphate; copper(I) sulfate pentahydrate; tetra(n-butyl)ammonium hydroxide; sodium L-ascorbate; In tetrahydrofuran; tert-butyl methyl ether; water;

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