{2-[6-amino-2-(4-hexyl-3-hydroxyphenylamino)-purine-9-yl]-ethoxymethyl}-phosphonic acid diethyl ester

Base Information

Chemical Name:{2-[6-amino-2-(4-hexyl-3-hydroxyphenylamino)-purine-9-yl]-ethoxymethyl}-phosphonic acid diethyl ester
CAS No.:1252577-04-0
Molecular Formula:C₂₄H₃₇N₆O₅P
Molecular Weight:520.569
Hs Code.:

Synonyms:{2-[6-amino-2-(4-hexyl-3-hydroxyphenylamino)-purine-9-yl]-ethoxymethyl}-phosphonic acid diethyl ester

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Chemical Property of {2-[6-amino-2-(4-hexyl-3-hydroxyphenylamino)-purine-9-yl]-ethoxymethyl}-phosphonic acid diethyl ester

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Technology Process of {2-[6-amino-2-(4-hexyl-3-hydroxyphenylamino)-purine-9-yl]-ethoxymethyl}-phosphonic acid diethyl ester

There total 12 articles about {2-[6-amino-2-(4-hexyl-3-hydroxyphenylamino)-purine-9-yl]-ethoxymethyl}-phosphonic acid diethyl 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: 40.0%

: 1252577-11-9
{2-[6-chloro-2-(4-hexyl-3-hydroxyphenylamino)-purin-9-yl]-ethoxymethyl}-phosphonic acid diethyl ester

: 1252577-04-0
{2-[6-amino-2-(4-hexyl-3-hydroxyphenylamino)-purine-9-yl]-ethoxymethyl}-phosphonic acid diethyl ester

Guidance literature:: With ammonia; In methanol; at 85 ℃; for 15h; Autoclave;
DOI:10.1016/j.ijpharm.2010.06.036

Reference yield:

: 1252577-05-1
3-(tert-butyldiphenylsiloxy)-4-hexylphenylamine

: 1252577-04-0
{2-[6-amino-2-(4-hexyl-3-hydroxyphenylamino)-purine-9-yl]-ethoxymethyl}-phosphonic acid diethyl ester

Guidance literature:: Multi-step reaction with 5 steps

1.1: ethyl methyl ether; water / 16 h / 125 °C

2.1: tetrabutyl-ammonium chloride; N,N-dimethyl-aniline; trichlorophosphate / acetonitrile / 8.5 h / 110 °C

2.2: 15.25 h / 0 °C

3.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 0.5 h / 20 °C

3.2: 17 h / 70 °C

4.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 2.5 h / 20 °C

5.1: ammonia / methanol / 15 h / 85 °C / Autoclave

With tetrabutyl ammonium fluoride; tetrabutyl-ammonium chloride; ammonia; N,N-dimethyl-aniline; 1,8-diazabicyclo[5.4.0]undec-7-ene; trichlorophosphate; In tetrahydrofuran; methanol; ethyl methyl ether; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/j.ijpharm.2010.06.036

Reference yield:

: 2-[3-(tert-butyldiphenylsiloxy)-4-hexylphenylamino]-1,4,5,9-tetrahydropurin-6-one

: 1252577-04-0
{2-[6-amino-2-(4-hexyl-3-hydroxyphenylamino)-purine-9-yl]-ethoxymethyl}-phosphonic acid diethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: tetrabutyl-ammonium chloride; N,N-dimethyl-aniline; trichlorophosphate / acetonitrile / 8.5 h / 110 °C

1.2: 15.25 h / 0 °C

2.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 0.5 h / 20 °C

2.2: 17 h / 70 °C

3.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 2.5 h / 20 °C

4.1: ammonia / methanol / 15 h / 85 °C / Autoclave

With tetrabutyl ammonium fluoride; tetrabutyl-ammonium chloride; ammonia; N,N-dimethyl-aniline; 1,8-diazabicyclo[5.4.0]undec-7-ene; trichlorophosphate; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1016/j.ijpharm.2010.06.036