1-(4-(benzylamino)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-2-yl)-2-methoxy-1H-benzo[d]imidazole-4-carboxamide

Base Information

Chemical Name:1-(4-(benzylamino)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-2-yl)-2-methoxy-1H-benzo[d]imidazole-4-carboxamide
CAS No.:1542706-09-1
Molecular Formula:C₂₃H₂₂N₆O₃
Molecular Weight:430.466
Hs Code.:

Synonyms:1-(4-(benzylamino)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-2-yl)-2-methoxy-1H-benzo[d]imidazole-4-carboxamide

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Chemical Property of 1-(4-(benzylamino)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-2-yl)-2-methoxy-1H-benzo[d]imidazole-4-carboxamide

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Technology Process of 1-(4-(benzylamino)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-2-yl)-2-methoxy-1H-benzo[d]imidazole-4-carboxamide

There total 8 articles about 1-(4-(benzylamino)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-2-yl)-2-methoxy-1H-benzo[d]imidazole-4-carboxamide 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: 62.0%

: 1542706-33-1
1-(4-(benzylamino)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-2-yl)-2-methoxy-1H-benzo[d]imidazole-4-carbonitrile

: 1542706-09-1
1-(4-(benzylamino)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-2-yl)-2-methoxy-1H-benzo[d]imidazole-4-carboxamide

Guidance literature:: With Acetaldehyde oxime; water; palladium diacetate; triphenylphosphine; In ethanol; at 80 ℃; for 12h;

Reference yield:

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

: 1542706-09-1
1-(4-(benzylamino)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-2-yl)-2-methoxy-1H-benzo[d]imidazole-4-carboxamide

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; potassium carbonate / 1,4-dioxane / 12 h / 100 °C / Inert atmosphere

7.1: palladium diacetate; water; triphenylphosphine; Acetaldehyde oxime / ethanol / 12 h / 80 °C

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; Acetaldehyde oxime; ammonium acetate; water; palladium diacetate; sodium hydride; potassium carbonate; triphenylphosphine; XPhos; trichlorophosphate; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; hexane; acetonitrile;

Reference yield:

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

: 1542706-09-1
1-(4-(benzylamino)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-2-yl)-2-methoxy-1H-benzo[d]imidazole-4-carboxamide

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; potassium carbonate / 1,4-dioxane / 12 h / 100 °C / Inert atmosphere

6.1: palladium diacetate; water; triphenylphosphine; Acetaldehyde oxime / ethanol / 12 h / 80 °C

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; Acetaldehyde oxime; ammonium acetate; water; palladium diacetate; potassium carbonate; triphenylphosphine; XPhos; trichlorophosphate; In 1,4-dioxane; methanol; ethanol; acetonitrile;