2-(2-((tert-butoxycarbonyl)(4-cyclohexylbenzyl)amino)-6-(cyclohexylamino)-9H-purin-9-yl)acetic acid

Base Information

Chemical Name:2-(2-((tert-butoxycarbonyl)(4-cyclohexylbenzyl)amino)-6-(cyclohexylamino)-9H-purin-9-yl)acetic acid
CAS No.:1255652-75-5
Molecular Formula:C₃₁H₄₂N₆O₄
Molecular Weight:562.712
Hs Code.:

Synonyms:2-(2-((tert-butoxycarbonyl)(4-cyclohexylbenzyl)amino)-6-(cyclohexylamino)-9H-purin-9-yl)acetic acid

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Chemical Property of 2-(2-((tert-butoxycarbonyl)(4-cyclohexylbenzyl)amino)-6-(cyclohexylamino)-9H-purin-9-yl)acetic acid

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Technology Process of 2-(2-((tert-butoxycarbonyl)(4-cyclohexylbenzyl)amino)-6-(cyclohexylamino)-9H-purin-9-yl)acetic acid

There total 9 articles about 2-(2-((tert-butoxycarbonyl)(4-cyclohexylbenzyl)amino)-6-(cyclohexylamino)-9H-purin-9-yl)acetic acid 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: 89.0%

: 1255652-40-4
ethyl 2-(2-((tert-butoxycarbonyl)(4-cyclohexylbenzyl)amino)-6-(cyclohexylamino)-9Hpurin-8-yl)acetate

: 1255652-75-5
2-(2-((tert-butoxycarbonyl)(4-cyclohexylbenzyl)amino)-6-(cyclohexylamino)-9H-purin-9-yl)acetic acid

Guidance literature:: With water; lithium hydroxide; In tetrahydrofuran; at 20 ℃; for 0.5h;
DOI:10.1021/ml100224d

Reference yield: 89.0%

: 1255652-75-5
2-(2-((tert-butoxycarbonyl)(4-cyclohexylbenzyl)amino)-6-(cyclohexylamino)-9H-purin-9-yl)acetic acid

Guidance literature:

Reference yield:

: 1236151-75-9
ethyl 2-(2-((tert-butoxycarbonyl)amino)-6-chloro-9H-purin-9-yl)acetate

: 1255652-75-5
2-(2-((tert-butoxycarbonyl)(4-cyclohexylbenzyl)amino)-6-(cyclohexylamino)-9H-purin-9-yl)acetic acid

Guidance literature:: Multi-step reaction with 3 steps

1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 20 °C / Inert atmosphere

2: N-ethyl-N,N-diisopropylamine / dimethyl sulfoxide / 0.5 h / 135 °C / Microwave irradiation; Sealed tube

3: water; lithium hydroxide / tetrahydrofuran / 0.5 h / 20 °C

With di-isopropyl azodicarboxylate; water; N-ethyl-N,N-diisopropylamine; triphenylphosphine; lithium hydroxide; In tetrahydrofuran; dimethyl sulfoxide; 1: Mitsunobu reaction;
DOI:10.1021/ml100224d