8-(3-{[5-(3-methoxyphenyl)-1,2,4-oxadiazol-3-yl]methoxy}-1-methyl-1H-pyrazol-5-yl)-1,3-dipropyl-3,7-dihydro-1H-purine-2,6-dione

Base Information

Chemical Name:8-(3-{[5-(3-methoxyphenyl)-1,2,4-oxadiazol-3-yl]methoxy}-1-methyl-1H-pyrazol-5-yl)-1,3-dipropyl-3,7-dihydro-1H-purine-2,6-dione
CAS No.:1354696-56-2
Molecular Formula:C₂₅H₂₈N₈O₅
Molecular Weight:520.548
Hs Code.:

Synonyms:8-(3-{[5-(3-methoxyphenyl)-1,2,4-oxadiazol-3-yl]methoxy}-1-methyl-1H-pyrazol-5-yl)-1,3-dipropyl-3,7-dihydro-1H-purine-2,6-dione

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Chemical Property of 8-(3-{[5-(3-methoxyphenyl)-1,2,4-oxadiazol-3-yl]methoxy}-1-methyl-1H-pyrazol-5-yl)-1,3-dipropyl-3,7-dihydro-1H-purine-2,6-dione

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Technology Process of 8-(3-{[5-(3-methoxyphenyl)-1,2,4-oxadiazol-3-yl]methoxy}-1-methyl-1H-pyrazol-5-yl)-1,3-dipropyl-3,7-dihydro-1H-purine-2,6-dione

There total 8 articles about 8-(3-{[5-(3-methoxyphenyl)-1,2,4-oxadiazol-3-yl]methoxy}-1-methyl-1H-pyrazol-5-yl)-1,3-dipropyl-3,7-dihydro-1H-purine-2,6-dione which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 85.0%

: 1354696-65-3
8-(3-{[5-(3-methoxyphenyl)-1,2,4-oxadiazol-3-yl]methoxy}-1-methyl-1H-pyrazol-5-yl)-1,3-dipropyl-7-{[2-(trimethylsilanyl)ethoxy]methyl}-3,7-dihydro-1H-purine-2,6-dione

: 1354696-56-2
8-(3-{[5-(3-methoxyphenyl)-1,2,4-oxadiazol-3-yl]methoxy}-1-methyl-1H-pyrazol-5-yl)-1,3-dipropyl-3,7-dihydro-1H-purine-2,6-dione

Guidance literature:: With hydrogenchloride; In ethanol; at 80 ℃; for 4h;
DOI:10.1021/jm201292w

Reference yield:

: 628329-62-4
methyl 3-(benzyloxy)-1-methyl-1H-pyrazole-5-carboxylate

: 1354696-56-2
8-(3-{[5-(3-methoxyphenyl)-1,2,4-oxadiazol-3-yl]methoxy}-1-methyl-1H-pyrazol-5-yl)-1,3-dipropyl-3,7-dihydro-1H-purine-2,6-dione

Guidance literature:: Multi-step reaction with 7 steps

1.1: potassium hydroxide / 1,4-dioxane; water / 6 h / 20 °C

1.2: pH 4 - 5

2.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / methanol / 18 h / 20 °C / Inert atmosphere

3.1: sodium hydroxide / 2 h / 80 °C

4.1: potassium carbonate / N,N-dimethyl-formamide / 72 h / 70 °C

5.1: palladium 10% on activated carbon; ammonium formate / methanol / 6 h / Reflux

6.1: potassium carbonate / acetone / 24 h / 60 °C

7.1: hydrogenchloride / ethanol / 4 h / 80 °C

With hydrogenchloride; palladium 10% on activated carbon; ammonium formate; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; potassium hydroxide; sodium hydroxide; In 1,4-dioxane; methanol; ethanol; water; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm201292w

Reference yield:

: 1354696-63-1
8-[(3-benzyloxy)-1-methyl-1H-pyrazol-5-yl]-1,3-dipropyl-7-(2-(trimethylsilanyl)ethoxymethyl)-3,7-dihydro-purine-2,6-dione

: 1354696-56-2
8-(3-{[5-(3-methoxyphenyl)-1,2,4-oxadiazol-3-yl]methoxy}-1-methyl-1H-pyrazol-5-yl)-1,3-dipropyl-3,7-dihydro-1H-purine-2,6-dione

Guidance literature:: Multi-step reaction with 3 steps

1: palladium 10% on activated carbon; ammonium formate / methanol / 6 h / Reflux

2: potassium carbonate / acetone / 24 h / 60 °C

3: hydrogenchloride / ethanol / 4 h / 80 °C

With hydrogenchloride; palladium 10% on activated carbon; ammonium formate; potassium carbonate; In methanol; ethanol; acetone;
DOI:10.1021/jm201292w