N-benzyl-2-(2-methyl-4-(1H-tetrazol-5-yl)-1H-indol-1-yl)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-amine

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Chemical Name:N-benzyl-2-(2-methyl-4-(1H-tetrazol-5-yl)-1H-indol-1-yl)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-amine
CAS No.:1542706-62-6
Molecular Formula:C₂₄H₂₂N₈O
Molecular Weight:438.492
Hs Code.:

Synonyms:N-benzyl-2-(2-methyl-4-(1H-tetrazol-5-yl)-1H-indol-1-yl)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-amine

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Chemical Property of N-benzyl-2-(2-methyl-4-(1H-tetrazol-5-yl)-1H-indol-1-yl)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-amine

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Technology Process of N-benzyl-2-(2-methyl-4-(1H-tetrazol-5-yl)-1H-indol-1-yl)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-amine

There total 7 articles about N-benzyl-2-(2-methyl-4-(1H-tetrazol-5-yl)-1H-indol-1-yl)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-amine 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: 11.0%

: 1542705-83-8
1-(4-(benzylamino)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-2-yl)-2-methyl-1H-indole-4-carbonitrile

: 1542706-62-6
N-benzyl-2-(2-methyl-4-(1H-tetrazol-5-yl)-1H-indol-1-yl)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-amine

Guidance literature:: With sodium azide; ammonium chloride; lithium chloride; In N,N-dimethyl-formamide; at 120 ℃; for 14h; Inert atmosphere;

Reference yield:

: 29943-42-8,143562-54-3
Tetrahydro-4H-pyran-4-one

: 1542706-62-6
N-benzyl-2-(2-methyl-4-(1H-tetrazol-5-yl)-1H-indol-1-yl)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium hydride / tetrahydrofuran; hexane / 45 °C

2.1: ammonium acetate / methanol / 20 °C

3.1: acetonitrile / 0.5 h

3.2: 70 °C

4.1: trichlorophosphate / 2 h / Reflux

5.1: acetonitrile / 20 °C

6.1: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; caesium carbonate / 1,4-dioxane / 2 h / 100 °C

7.1: ammonium chloride; sodium azide; lithium chloride / N,N-dimethyl-formamide / 14 h / 120 °C / Inert atmosphere

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; sodium azide; ammonium acetate; sodium hydride; ammonium chloride; caesium carbonate; lithium chloride; XPhos; trichlorophosphate; In tetrahydrofuran; 1,4-dioxane; methanol; hexane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 127956-11-0
4-oxotetrahydro-2H-pyran-3-carboxylic acid methyl ester

: 1542706-62-6
N-benzyl-2-(2-methyl-4-(1H-tetrazol-5-yl)-1H-indol-1-yl)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 6 steps

1.1: ammonium acetate / methanol / 20 °C

2.1: acetonitrile / 0.5 h

2.2: 70 °C

3.1: trichlorophosphate / 2 h / Reflux

4.1: acetonitrile / 20 °C

5.1: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; caesium carbonate / 1,4-dioxane / 2 h / 100 °C

6.1: ammonium chloride; sodium azide; lithium chloride / N,N-dimethyl-formamide / 14 h / 120 °C / Inert atmosphere

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; sodium azide; ammonium acetate; ammonium chloride; caesium carbonate; lithium chloride; XPhos; trichlorophosphate; In 1,4-dioxane; methanol; N,N-dimethyl-formamide; acetonitrile;