1-(1-acryloylpiperidin-3-yl)-5-(methylamino)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamide

Base Information

Chemical Name:1-(1-acryloylpiperidin-3-yl)-5-(methylamino)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamide
CAS No.:1612773-99-5
Molecular Formula:C₂₅H₂₇N₅O₃
Molecular Weight:445.521
Hs Code.:

Synonyms:1-(1-acryloylpiperidin-3-yl)-5-(methylamino)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamide

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Chemical Property of 1-(1-acryloylpiperidin-3-yl)-5-(methylamino)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamide

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Technology Process of 1-(1-acryloylpiperidin-3-yl)-5-(methylamino)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamide

There total 13 articles about 1-(1-acryloylpiperidin-3-yl)-5-(methylamino)-3-(4-phenoxyphenyl)-1H-pyrazole-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:

: 330792-69-3
2-[(4-phenoxy-phenyl)-methoxy-methylene]-malononitrile

: 1612773-99-5
1-(1-acryloylpiperidin-3-yl)-5-(methylamino)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: hydrazine hydrate / ethanol / 2 h / 20 - 90 °C

2.1: caesium carbonate / N,N-dimethyl-formamide / 50 h / 20 - 80 °C

3.1: dmap; triethylamine / tetrahydrofuran / 0 - 20 °C

4.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.33 h / 0 - 20 °C

4.2: 1 h / 20 - 60 °C

5.1: potassium carbonate; dihydrogen peroxide / dimethyl sulfoxide / 1 h / 20 - 60 °C

6.1: hydrogenchloride / 1,4-dioxane / 20 °C

6.2: 0.08 h / 0 °C

With hydrogenchloride; dmap; hydrazine hydrate; dihydrogen peroxide; sodium hydride; potassium carbonate; caesium carbonate; triethylamine; In tetrahydrofuran; 1,4-dioxane; ethanol; dimethyl sulfoxide; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 1612774-47-6
tert-butyl 3-(5-amino-4-cyano-3-(4-phenoxyphenyl)-1H-pyrazol-1-yl)-piperidine-1-carboxylate

: 1612773-99-5
1-(1-acryloylpiperidin-3-yl)-5-(methylamino)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: dmap; triethylamine / tetrahydrofuran / 0 - 20 °C

2.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.33 h / 0 - 20 °C

2.2: 1 h / 20 - 60 °C

3.1: potassium carbonate; dihydrogen peroxide / dimethyl sulfoxide / 1 h / 20 - 60 °C

4.1: hydrogenchloride / 1,4-dioxane / 20 °C

4.2: 0.08 h / 0 °C

With hydrogenchloride; dmap; dihydrogen peroxide; sodium hydride; potassium carbonate; triethylamine; In tetrahydrofuran; 1,4-dioxane; dimethyl sulfoxide; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 85275-45-2
N-tert-butoxycarbonyl-3-piperidinol

: 1612773-99-5
1-(1-acryloylpiperidin-3-yl)-5-(methylamino)-3-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: dmap; triethylamine / dichloromethane / 0 - 20 °C

2.1: caesium carbonate / N,N-dimethyl-formamide / 50 h / 20 - 80 °C

3.1: dmap; triethylamine / tetrahydrofuran / 0 - 20 °C

4.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.33 h / 0 - 20 °C

4.2: 1 h / 20 - 60 °C

5.1: potassium carbonate; dihydrogen peroxide / dimethyl sulfoxide / 1 h / 20 - 60 °C

6.1: hydrogenchloride / 1,4-dioxane / 20 °C

6.2: 0.08 h / 0 °C

With hydrogenchloride; dmap; dihydrogen peroxide; sodium hydride; potassium carbonate; caesium carbonate; triethylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; mineral oil;