5-ethylcarboxyamide-2-(6'-amino-2'-(3''-(1''-(p-toluenesulfonyl)indolyl)ethyloxy)-purin-9'-yl)-tetrahydrofuran

Base Information

Chemical Name:5-ethylcarboxyamide-2-(6'-amino-2'-(3''-(1''-(p-toluenesulfonyl)indolyl)ethyloxy)-purin-9'-yl)-tetrahydrofuran
CAS No.:936252-46-9
Molecular Formula:C₂₉H₃₁N₇O₇S
Molecular Weight:621.674
Hs Code.:

Synonyms:5-ethylcarboxyamide-2-(6'-amino-2'-(3''-(1''-(p-toluenesulfonyl)indolyl)ethyloxy)-purin-9'-yl)-tetrahydrofuran

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Chemical Property of 5-ethylcarboxyamide-2-(6'-amino-2'-(3''-(1''-(p-toluenesulfonyl)indolyl)ethyloxy)-purin-9'-yl)-tetrahydrofuran

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Technology Process of 5-ethylcarboxyamide-2-(6'-amino-2'-(3''-(1''-(p-toluenesulfonyl)indolyl)ethyloxy)-purin-9'-yl)-tetrahydrofuran

There total 10 articles about 5-ethylcarboxyamide-2-(6'-amino-2'-(3''-(1''-(p-toluenesulfonyl)indolyl)ethyloxy)-purin-9'-yl)-tetrahydrofuran 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: 85.0%

: 936253-03-1
5-ethylcarboxyamide-2-(6'-amino-2'-(3''-(1''-(p-toluenesulfonyl)indolyl)ethyloxy)-purin-9'-yl)-3,4-O-isopropylidene-tetrahydrofuran

: 936252-46-9
5-ethylcarboxyamide-2-(6'-amino-2'-(3''-(1''-(p-toluenesulfonyl)indolyl)ethyloxy)-purin-9'-yl)-tetrahydrofuran

Guidance literature:: With water; acetic acid; at 80 ℃; for 63h;

Reference yield:

: 1026746-27-9
(1-tosyl-1H-indol-3-yl)ethyl-4-methylbenzenesulfonate

: 936252-46-9
5-ethylcarboxyamide-2-(6'-amino-2'-(3''-(1''-(p-toluenesulfonyl)indolyl)ethyloxy)-purin-9'-yl)-tetrahydrofuran

Guidance literature:: Multi-step reaction with 4 steps

1: 57 percent / sodium iodide / dimethylformamide / 60 °C

2: 70 percent / cesium carbonate / dimethylformamide / 20 °C

3: 88 percent / NH₃ / ethanol / 120 °C

4: 9 mg / aq. acetic acid / 63 h / 80 °C

With ammonia; caesium carbonate; acetic acid; sodium iodide; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm061278q

Reference yield:

: 936252-49-2
3-(2-iodoethyl)-1-(p-toluenesulfonyl)indole

: 936252-46-9
5-ethylcarboxyamide-2-(6'-amino-2'-(3''-(1''-(p-toluenesulfonyl)indolyl)ethyloxy)-purin-9'-yl)-tetrahydrofuran

Guidance literature:: Multi-step reaction with 3 steps

1: 70 percent / cesium carbonate / dimethylformamide / 20 °C

2: 88 percent / NH₃ / ethanol / 120 °C

3: 9 mg / aq. acetic acid / 63 h / 80 °C

With ammonia; caesium carbonate; acetic acid; In ethanol; N,N-dimethyl-formamide;
DOI:10.1021/jm061278q