(2S,3R,4S,5R)-2-(4-amino-3-phenylpyrazolo[3,4-d]pyrimidin-1-yl)-5-hydroxymethyltetrahydrofuran-3,4-diol

Base Information

Chemical Name:(2S,3R,4S,5R)-2-(4-amino-3-phenylpyrazolo[3,4-d]pyrimidin-1-yl)-5-hydroxymethyltetrahydrofuran-3,4-diol
CAS No.:476371-75-2
Molecular Formula:C₁₆H₁₇N₅O₄
Molecular Weight:343.342
Hs Code.:

Synonyms:(2S,3R,4S,5R)-2-(4-amino-3-phenylpyrazolo[3,4-d]pyrimidin-1-yl)-5-hydroxymethyltetrahydrofuran-3,4-diol

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Chemical Property of (2S,3R,4S,5R)-2-(4-amino-3-phenylpyrazolo[3,4-d]pyrimidin-1-yl)-5-hydroxymethyltetrahydrofuran-3,4-diol

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Technology Process of (2S,3R,4S,5R)-2-(4-amino-3-phenylpyrazolo[3,4-d]pyrimidin-1-yl)-5-hydroxymethyltetrahydrofuran-3,4-diol

There total 6 articles about (2S,3R,4S,5R)-2-(4-amino-3-phenylpyrazolo[3,4-d]pyrimidin-1-yl)-5-hydroxymethyltetrahydrofuran-3,4-diol 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: 34.0%

: 90914-42-4
4-amino-3-bromo-1-β-D-ribofuranosylpyrazolo<3,4-d>pyrimidine

: 98-80-6
phenylboronic acid

: 476371-75-2
(2S,3R,4S,5R)-2-(4-amino-3-phenylpyrazolo[3,4-d]pyrimidin-1-yl)-5-hydroxymethyltetrahydrofuran-3,4-diol

Guidance literature:: With trisodium tris(3-sulfophenyl)phosphine; palladium diacetate; sodium carbonate; In water; acetonitrile; Inert atmosphere; Reflux;
DOI:10.1021/acs.jmedchem.1c00135

Reference yield:

: 46177-21-3
2-benzoylmalononitrile

: 476371-75-2
(2S,3R,4S,5R)-2-(4-amino-3-phenylpyrazolo[3,4-d]pyrimidin-1-yl)-5-hydroxymethyltetrahydrofuran-3,4-diol

Guidance literature:: Multi-step reaction with 5 steps

1: 84 percent / aq. NaHCO₃ / dioxane / Heating

2: 75 percent / hydrazine hydrochloride; triethylamine / ethanol / Heating

3: 72 percent / 180 °C

4: 70 percent / SnCl₄ / acetonitrile / 20 °C

5: 81 percent / NH₃ / methanol / 20 °C

With hydrazine hydrochloride; ammonia; tin(IV) chloride; sodium hydrogencarbonate; triethylamine; In 1,4-dioxane; methanol; ethanol; acetonitrile;
DOI:10.1021/ja0264798

Reference yield:

: 42754-56-3
2-(methoxyphenylmethylene)malononitrile

: 476371-75-2
(2S,3R,4S,5R)-2-(4-amino-3-phenylpyrazolo[3,4-d]pyrimidin-1-yl)-5-hydroxymethyltetrahydrofuran-3,4-diol

Guidance literature:: Multi-step reaction with 4 steps

1: 75 percent / hydrazine hydrochloride; triethylamine / ethanol / Heating

2: 72 percent / 180 °C

3: 70 percent / SnCl₄ / acetonitrile / 20 °C

4: 81 percent / NH₃ / methanol / 20 °C

With hydrazine hydrochloride; ammonia; tin(IV) chloride; triethylamine; In methanol; ethanol; acetonitrile;
DOI:10.1021/ja0264798