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N6-(2-methylbenzyl)-2'-deoxy-2'-aminoadenosine

Base Information Edit
  • Chemical Name:N6-(2-methylbenzyl)-2'-deoxy-2'-aminoadenosine
  • CAS No.:1054631-71-8
  • Molecular Formula:C18H22N6O3
  • Molecular Weight:370.411
  • Hs Code.:
  • Mol file:1054631-71-8.mol
N<sup>6</sup>-(2-methylbenzyl)-2'-deoxy-2'-aminoadenosine

Synonyms:N6-(2-methylbenzyl)-2'-deoxy-2'-aminoadenosine

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Chemical Property of N6-(2-methylbenzyl)-2'-deoxy-2'-aminoadenosine Edit
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Technology Process of N6-(2-methylbenzyl)-2'-deoxy-2'-aminoadenosine

There total 6 articles about N6-(2-methylbenzyl)-2'-deoxy-2'-aminoadenosine 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:
Guidance literature:
Multi-step reaction with 6 steps
1: 99 percent / adenosine deaminase; H2O / 20 °C
2: dimethylformamide / 3 h / 60 °C
3: Et3N; DMAP / acetonitrile / 1 h / 20 °C
4: 92 percent / POCl3; Et4NCl; N,N-dimethylaniline / acetonitrile / 0.17 h / 100 °C
5: Et3N / ethanol / 18 h / 60 °C
6: aq. NH3 / ethanol / 24 h / 80 °C
With dmap; ammonium hydroxide; tetraethylammonium chloride; water; N,N-dimethyl-aniline; triethylamine; adenosine deaminase; trichlorophosphate; In ethanol; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm000472o
Guidance literature:
Multi-step reaction with 5 steps
1: dimethylformamide / 3 h / 60 °C
2: Et3N; DMAP / acetonitrile / 1 h / 20 °C
3: 92 percent / POCl3; Et4NCl; N,N-dimethylaniline / acetonitrile / 0.17 h / 100 °C
4: Et3N / ethanol / 18 h / 60 °C
5: aq. NH3 / ethanol / 24 h / 80 °C
With dmap; ammonium hydroxide; tetraethylammonium chloride; N,N-dimethyl-aniline; triethylamine; trichlorophosphate; In ethanol; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jm000472o
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