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

Base Information

Chemical Name:(R)-1-(1-acryloylpiperidin-3-yl)-3-amino-5-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamide
CAS No.:1612774-15-8
Molecular Formula:C₂₄H₂₅N₅O₃
Molecular Weight:431.494
Hs Code.:

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

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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

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

There total 13 articles about (R)-1-(1-acryloylpiperidin-3-yl)-3-amino-5-(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: 26.0%

: 1612774-55-6
(R)-3-amino-5-(4-phenoxyphenyl)-1-(piperidin-3-yl)-1H-pyrazole-4-carboxamide

: 814-68-6,25189-84-8
acryloyl chloride

: 1612774-15-8
(R)-1-(1-acryloylpiperidin-3-yl)-3-amino-5-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamide

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 0.0833333h;

Reference yield:

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

: 1612774-15-8
(R)-1-(1-acryloylpiperidin-3-yl)-3-amino-5-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

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

2: caesium carbonate / N,N-dimethyl-formamide / 5 h / 20 - 80 °C

3: potassium carbonate; dihydrogen peroxide / dimethyl sulfoxide / 5 h / 20 - 60 °C

4: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

5: triethylamine / dichloromethane / 0.08 h / 0 °C

With hydrazine hydrate; dihydrogen peroxide; potassium carbonate; caesium carbonate; triethylamine; trifluoroacetic acid; In ethanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 143900-44-1
tert-butyl (3S)-3-hydroxypiperidine-1-carboxylate

: 1612774-15-8
(R)-1-(1-acryloylpiperidin-3-yl)-3-amino-5-(4-phenoxyphenyl)-1H-pyrazole-4-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: dmap; triethylamine / dichloromethane / 40 h / 0 - 20 °C

2: caesium carbonate / N,N-dimethyl-formamide / 5 h / 20 - 80 °C

3: potassium carbonate; dihydrogen peroxide / dimethyl sulfoxide / 5 h / 20 - 60 °C

4: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

5: triethylamine / dichloromethane / 0.08 h / 0 °C

With dmap; dihydrogen peroxide; potassium carbonate; caesium carbonate; triethylamine; trifluoroacetic acid; In dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide;