2-(2-chloro-9-(4-methoxybenzyl)-6-oxo-6,9-dihydro-1H-purin-1-yl)acetonitrile

Base Information

Chemical Name:2-(2-chloro-9-(4-methoxybenzyl)-6-oxo-6,9-dihydro-1H-purin-1-yl)acetonitrile
CAS No.:1417715-69-5
Molecular Formula:C₁₅H₁₂ClN₅O₂
Molecular Weight:329.746
Hs Code.:

Synonyms:2-(2-chloro-9-(4-methoxybenzyl)-6-oxo-6,9-dihydro-1H-purin-1-yl)acetonitrile

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Chemical Property of 2-(2-chloro-9-(4-methoxybenzyl)-6-oxo-6,9-dihydro-1H-purin-1-yl)acetonitrile

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Technology Process of 2-(2-chloro-9-(4-methoxybenzyl)-6-oxo-6,9-dihydro-1H-purin-1-yl)acetonitrile

There total 4 articles about 2-(2-chloro-9-(4-methoxybenzyl)-6-oxo-6,9-dihydro-1H-purin-1-yl)acetonitrile 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: 55.0%

: 2-chloro-9-(4-methoxybenzyl)-1,9-dihydro-6H-purin-6-one

: 590-17-0
cyanomethyl bromide

: 1417715-69-5
2-(2-chloro-9-(4-methoxybenzyl)-6-oxo-6,9-dihydro-1H-purin-1-yl)acetonitrile

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 50 ℃; for 2h;

Reference yield:

: 115204-74-5
2,6-dichloro-9-(4-methoxyphenylmethyl)-9H-purine

: 1417715-69-5
2-(2-chloro-9-(4-methoxybenzyl)-6-oxo-6,9-dihydro-1H-purin-1-yl)acetonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / 2 h / Reflux

2: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 2 h / 50 °C

With N-ethyl-N,N-diisopropylamine; sodium hydroxide; In N,N-dimethyl-formamide;
DOI:10.1021/acsmedchemlett.6b00027

Reference yield:

: 5451-40-1
2,6-dichloro-7H-purine

: 1417715-69-5
2-(2-chloro-9-(4-methoxybenzyl)-6-oxo-6,9-dihydro-1H-purin-1-yl)acetonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / N,N-dimethyl-formamide / 21 h / 20 °C

2: sodium hydroxide / 2 h / Reflux

3: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 2 h / 50 °C

With potassium carbonate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In N,N-dimethyl-formamide;