N-(cyanomethyl)-4-(2-(4-(d₈-morpholino)phenylamino)pyrimidin-4-yl) benzamide

Base Information

Chemical Name:N-(cyanomethyl)-4-(2-(4-(d₈-morpholino)phenylamino)pyrimidin-4-yl) benzamide
CAS No.:1619927-68-2
Molecular Formula:C₂₃H₂₂N₆O₂
Molecular Weight:422.403
Hs Code.:

N-(cyanomethyl)-4-(2-(4-(d<SUB>8</SUB>-morpholino)phenylamino)pyrimidin-4-yl) benzamide

Synonyms:N-(cyanomethyl)-4-(2-(4-(d₈-morpholino)phenylamino)pyrimidin-4-yl) benzamide

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Chemical Property of N-(cyanomethyl)-4-(2-(4-(d₈-morpholino)phenylamino)pyrimidin-4-yl) benzamide

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Technology Process of N-(cyanomethyl)-4-(2-(4-(d₈-morpholino)phenylamino)pyrimidin-4-yl) benzamide

There total 5 articles about N-(cyanomethyl)-4-(2-(4-(d₈-morpholino)phenylamino)pyrimidin-4-yl) benzamide 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: 40.0%

: 4-(2-(4-(d₈-morpholino)phenylamino)pyrimidin-4-yl)methyl benzoate

: 6011-14-9
2-aminoacetonitrile hydrochloride

: 1619927-68-2
N-(cyanomethyl)-4-(2-(4-(d₈-morpholino)phenylamino)pyrimidin-4-yl) benzamide

Guidance literature:: With potassium carbonate; In tetrahydrofuran; at 35 ℃;

Reference yield:

: 1115228-37-9
4-(4-nitrophenyl)-d₈-morpholine

: 1619927-68-2
N-(cyanomethyl)-4-(2-(4-(d₈-morpholino)phenylamino)pyrimidin-4-yl) benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogen; palladium 10% on activated carbon / methanol / 20 h / 40 °C

2: toluene-4-sulfonic acid / water; 1,4-dioxane / 20 h / Reflux

3: potassium carbonate / tetrahydrofuran / 35 °C

With palladium 10% on activated carbon; hydrogen; potassium carbonate; toluene-4-sulfonic acid; In tetrahydrofuran; 1,4-dioxane; methanol; water;

Reference yield:

: 100-00-5
4-chlorobenzonitrile

: 1619927-68-2
N-(cyanomethyl)-4-(2-(4-(d₈-morpholino)phenylamino)pyrimidin-4-yl) benzamide

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / dimethyl sulfoxide / 16 h / 100 °C

2: hydrogen; palladium 10% on activated carbon / methanol / 20 h / 40 °C

3: toluene-4-sulfonic acid / water; 1,4-dioxane / 20 h / Reflux

4: potassium carbonate / tetrahydrofuran / 35 °C

With palladium 10% on activated carbon; hydrogen; potassium carbonate; toluene-4-sulfonic acid; In tetrahydrofuran; 1,4-dioxane; methanol; water; dimethyl sulfoxide;