2-{3-[4-(2,6-dioxo-1,3-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)pyrazol-1-yl]prop-1-ynyl}benzoic acid methyl ester

Base Information

Chemical Name:2-{3-[4-(2,6-dioxo-1,3-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)pyrazol-1-yl]prop-1-ynyl}benzoic acid methyl ester
CAS No.:1188540-92-2
Molecular Formula:C₂₅H₂₆N₆O₄
Molecular Weight:474.519
Hs Code.:

Synonyms:2-{3-[4-(2,6-dioxo-1,3-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)pyrazol-1-yl]prop-1-ynyl}benzoic acid methyl ester

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Chemical Property of 2-{3-[4-(2,6-dioxo-1,3-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)pyrazol-1-yl]prop-1-ynyl}benzoic acid methyl ester

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Technology Process of 2-{3-[4-(2,6-dioxo-1,3-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)pyrazol-1-yl]prop-1-ynyl}benzoic acid methyl ester

There total 7 articles about 2-{3-[4-(2,6-dioxo-1,3-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)pyrazol-1-yl]prop-1-ynyl}benzoic acid methyl ester 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:

: C₃₁H₄₀N₆O₅Si

: 1188540-92-2
2-{3-[4-(2,6-dioxo-1,3-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)pyrazol-1-yl]prop-1-ynyl}benzoic acid methyl ester

Guidance literature:: With hydrogenchloride; In ethanol; at 80 ℃; for 2h;
DOI:10.1016/j.ejmech.2017.04.014

Reference yield:

: 81250-34-2
1,3-dipropyl-5,6-diaminouracil

: 1188540-92-2
2-{3-[4-(2,6-dioxo-1,3-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)pyrazol-1-yl]prop-1-ynyl}benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / methanol / 20 °C

2: sodium hydroxide / methanol / Reflux

3: potassium carbonate / N,N-dimethyl-formamide / 20 °C

4: hydrogen; palladium 10% on activated carbon / dichloromethane; methanol / 20 °C

5: potassium carbonate / acetone / 5 h / Reflux

6: hydrogenchloride / ethanol / 2 h / 80 °C

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1016/j.ejmech.2017.04.014

Reference yield:

: 531506-36-2
8-(1-benzylpyrazol-4-yl)-1,3-dipropyl-1,3,7-trihydropurine-2,6-dione

: 1188540-92-2
2-{3-[4-(2,6-dioxo-1,3-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)pyrazol-1-yl]prop-1-ynyl}benzoic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / N,N-dimethyl-formamide / 20 °C

2: hydrogen; palladium 10% on activated carbon / dichloromethane; methanol / 20 °C

3: potassium carbonate / acetone / 5 h / Reflux

4: hydrogenchloride / ethanol / 2 h / 80 °C

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; potassium carbonate; In methanol; ethanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1016/j.ejmech.2017.04.014