2-[2-(6-amino-2-chloro-purin-9-yl)-ethyl]-2-ethoxycarbonyl-malonic acid diethyl ester

Base Information

Chemical Name:2-[2-(6-amino-2-chloro-purin-9-yl)-ethyl]-2-ethoxycarbonyl-malonic acid diethyl ester
CAS No.:1026432-70-1
Molecular Formula:C₁₇H₂₂ClN₅O₆
Molecular Weight:427.845
Hs Code.:

Synonyms:2-[2-(6-amino-2-chloro-purin-9-yl)-ethyl]-2-ethoxycarbonyl-malonic acid diethyl ester

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Chemical Property of 2-[2-(6-amino-2-chloro-purin-9-yl)-ethyl]-2-ethoxycarbonyl-malonic acid diethyl ester

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Technology Process of 2-[2-(6-amino-2-chloro-purin-9-yl)-ethyl]-2-ethoxycarbonyl-malonic acid diethyl ester

There total 1 articles about 2-[2-(6-amino-2-chloro-purin-9-yl)-ethyl]-2-ethoxycarbonyl-malonic 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:

: 71170-82-6
triethyl 3-bromopropane-1,1,1-tricarboxylate

: 1839-18-5
2-chloroadenine

: 1026432-70-1
2-[2-(6-amino-2-chloro-purin-9-yl)-ethyl]-2-ethoxycarbonyl-malonic acid diethyl ester

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 60 ℃; for 24h;
DOI:10.1021/jm9905211

Reference yield:

: 1026432-70-1
2-[2-(6-amino-2-chloro-purin-9-yl)-ethyl]-2-ethoxycarbonyl-malonic acid diethyl ester

: 1027038-73-8
2-[2-(6-amino-2-chloro-purin-9-yl)-ethyl]-propane-1,3-bisoxy(dibenzylphosphate)

Guidance literature:: Multi-step reaction with 3 steps

1: 80 percent / methanol / 3 h

2: 74 percent / NaBH₄ / CH₂Cl₂; methanol / 4 h / 25 °C

3: 24 percent / lithium diisopropylamide / tetrahydrofuran / 13 h / -78 - 25 °C

With sodium tetrahydroborate; lithium diisopropyl amide; In tetrahydrofuran; methanol; dichloromethane; 1: Decarboxylation / 2: Reduction / 3: phosphorylation;
DOI:10.1021/jm9905211