2-({1-[(2S)-2-hydroxypropanoyl]piperidin-4-yl}oxy)-5-(2-{[4-(morpholin-4-yl)phenyl]amino}pyrimidin-4-yl)benzonitrile

Base Information

Chemical Name:2-({1-[(2S)-2-hydroxypropanoyl]piperidin-4-yl}oxy)-5-(2-{[4-(morpholin-4-yl)phenyl]amino}pyrimidin-4-yl)benzonitrile
CAS No.:1292310-50-9
Molecular Formula:C₂₉H₃₂N₆O₄
Molecular Weight:528.611
Hs Code.:

Synonyms:2-({1-[(2S)-2-hydroxypropanoyl]piperidin-4-yl}oxy)-5-(2-{[4-(morpholin-4-yl)phenyl]amino}pyrimidin-4-yl)benzonitrile

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Chemical Property of 2-({1-[(2S)-2-hydroxypropanoyl]piperidin-4-yl}oxy)-5-(2-{[4-(morpholin-4-yl)phenyl]amino}pyrimidin-4-yl)benzonitrile

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Technology Process of 2-({1-[(2S)-2-hydroxypropanoyl]piperidin-4-yl}oxy)-5-(2-{[4-(morpholin-4-yl)phenyl]amino}pyrimidin-4-yl)benzonitrile

There total 6 articles about 2-({1-[(2S)-2-hydroxypropanoyl]piperidin-4-yl}oxy)-5-(2-{[4-(morpholin-4-yl)phenyl]amino}pyrimidin-4-yl)benzonitrile 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:

: 79-33-4,106989-11-1,26811-96-1,31587-11-8,26100-51-6
L-Lactic acid

: 1292317-59-9
tert-butyl 4-[2-cyano-4-(2-{[4-(morpholin-4-yl)phenyl]amino}pyrimidin-4-yl)phenoxy]piperidine-1-carboxylate

: 1292310-50-9
2-({1-[(2S)-2-hydroxypropanoyl]piperidin-4-yl}oxy)-5-(2-{[4-(morpholin-4-yl)phenyl]amino}pyrimidin-4-yl)benzonitrile

Guidance literature:: With O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; In dichloromethane; at 20 ℃; for 18h;

Reference yield:

: 109384-19-2
t-butyl 4-hydroxy piperidine-1-carboxylate

: 1292310-50-9
2-({1-[(2S)-2-hydroxypropanoyl]piperidin-4-yl}oxy)-5-(2-{[4-(morpholin-4-yl)phenyl]amino}pyrimidin-4-yl)benzonitrile

Guidance literature:: Multi-step reaction with 5 steps

1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 18 h / 20 °C

2: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane / 20 h / 80 °C

3: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / acetonitrile; water / 20 h / Reflux

4: 1,4-dioxane; ethanol / 48 h / Reflux

5: triethylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / dichloromethane / 18 h / 20 °C

With potassium acetate; potassium carbonate; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; triphenylphosphine; diethylazodicarboxylate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; acetonitrile;

Reference yield:

: 1292317-56-6
tert-butyl 4-(4-bromo-2-cyanophenoxy)piperidine-1-carboxylate

: 1292310-50-9
2-({1-[(2S)-2-hydroxypropanoyl]piperidin-4-yl}oxy)-5-(2-{[4-(morpholin-4-yl)phenyl]amino}pyrimidin-4-yl)benzonitrile

Guidance literature:: Multi-step reaction with 4 steps

1: potassium acetate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane / 20 h / 80 °C

2: potassium carbonate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / acetonitrile; water / 20 h / Reflux

3: 1,4-dioxane; ethanol / 48 h / Reflux

4: triethylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / dichloromethane / 18 h / 20 °C

With potassium acetate; potassium carbonate; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,4-dioxane; ethanol; dichloromethane; water; acetonitrile;