2-amino-7-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-5-tosyl-5H-pyrrolo[3,2-d]pyrimidin-4-ol

Base Information

Chemical Name:2-amino-7-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-5-tosyl-5H-pyrrolo[3,2-d]pyrimidin-4-ol
CAS No.:1196886-19-7
Molecular Formula:C₂₂H₂₃N₅O₄S
Molecular Weight:453.522
Hs Code.:

Synonyms:2-amino-7-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-5-tosyl-5H-pyrrolo[3,2-d]pyrimidin-4-ol

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Chemical Property of 2-amino-7-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-5-tosyl-5H-pyrrolo[3,2-d]pyrimidin-4-ol

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Technology Process of 2-amino-7-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-5-tosyl-5H-pyrrolo[3,2-d]pyrimidin-4-ol

There total 9 articles about 2-amino-7-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-5-tosyl-5H-pyrrolo[3,2-d]pyrimidin-4-ol 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: 64.0%

: 1196886-17-5
7-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-2-(methylsulfonyl)-5-tosyl-5H-pyrrolo[3,2-d]pyrimidin-4-ol

: 1196886-19-7
2-amino-7-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-5-tosyl-5H-pyrrolo[3,2-d]pyrimidin-4-ol

Guidance literature:: With ammonia; In 1,4-dioxane; at 160 ℃; for 0.2h; under 7600.51 Torr;

Reference yield:

: 110464-72-7
4-methoxy-3,5-dimethyl-2-pyridinecarboxaldehyde

: 1196886-19-7
2-amino-7-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-5-tosyl-5H-pyrrolo[3,2-d]pyrimidin-4-ol

Guidance literature:: Multi-step reaction with 7 steps

1: potassium carbonate / ethanol / 4 h / 70 °C

2: Diisobutyl adipate / tetrahydrofuran / -78 - -7 °C

3: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 0 - 20 °C

4: potassium acetate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / toluene / 0.33 h / 180 °C / Microwave irradiation

5: oxone / dichloromethane / 36 h / 20 °C

6: hydrogen / palladium on activated charcoal / methanol / 12 h / 20 °C

7: ammonia / 1,4-dioxane / 0.2 h / 160 °C / 7600.51 Torr

With oxone; Diisobutyl adipate; ammonia; hydrogen; potassium acetate; potassium carbonate; triphenylphosphine; diethylazodicarboxylate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; dichloromethane; toluene;

Reference yield:

: 86604-78-6
(4-methoxy-3,5-dimethylpyridin-2-yl)methanol

: 1196886-19-7
2-amino-7-((4-methoxy-3,5-dimethylpyridin-2-yl)methyl)-5-tosyl-5H-pyrrolo[3,2-d]pyrimidin-4-ol

Guidance literature:: Multi-step reaction with 8 steps

1: manganese(IV) oxide / chloroform / 0.17 h / 20 °C

2: potassium carbonate / ethanol / 4 h / 70 °C

3: Diisobutyl adipate / tetrahydrofuran / -78 - -7 °C

4: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 0 - 20 °C

5: potassium acetate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / toluene / 0.33 h / 180 °C / Microwave irradiation

6: oxone / dichloromethane / 36 h / 20 °C

7: hydrogen / palladium on activated charcoal / methanol / 12 h / 20 °C

8: ammonia / 1,4-dioxane / 0.2 h / 160 °C / 7600.51 Torr

With manganese(IV) oxide; oxone; Diisobutyl adipate; ammonia; hydrogen; potassium acetate; potassium carbonate; triphenylphosphine; diethylazodicarboxylate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; palladium on activated charcoal; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; dichloromethane; chloroform; toluene;