(S)-5-amino-3-(4-(2,4-difluorophenoxy)phenyl)-1-(piperidin-3-yl)-1H-pyrazole-4-carboxamide

Base Information

Chemical Name:(S)-5-amino-3-(4-(2,4-difluorophenoxy)phenyl)-1-(piperidin-3-yl)-1H-pyrazole-4-carboxamide
CAS No.:1609468-25-8
Molecular Formula:C₂₁H₂₁F₂N₅O₂
Molecular Weight:413.427
Hs Code.:

Synonyms:(S)-5-amino-3-(4-(2,4-difluorophenoxy)phenyl)-1-(piperidin-3-yl)-1H-pyrazole-4-carboxamide

Suppliers and Price of (S)-5-amino-3-(4-(2,4-difluorophenoxy)phenyl)-1-(piperidin-3-yl)-1H-pyrazole-4-carboxamide

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of (S)-5-amino-3-(4-(2,4-difluorophenoxy)phenyl)-1-(piperidin-3-yl)-1H-pyrazole-4-carboxamide

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Hazard Codes:

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Technology Process of (S)-5-amino-3-(4-(2,4-difluorophenoxy)phenyl)-1-(piperidin-3-yl)-1H-pyrazole-4-carboxamide

There total 13 articles about (S)-5-amino-3-(4-(2,4-difluorophenoxy)phenyl)-1-(piperidin-3-yl)-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:

: 1609467-68-6
5-amino-3-(4-(2,4-difluorophenoxy)phenyl)-1-(piperidin-3-yl)-1H-pyrazole-4-carboxamide

: 1609468-25-8
(S)-5-amino-3-(4-(2,4-difluorophenoxy)phenyl)-1-(piperidin-3-yl)-1H-pyrazole-4-carboxamide

Guidance literature:: With (ChiralPak OJ-H,; In ethanol; isopropyl alcohol;

Reference yield:

: 1044060-43-6
methyl 4-(2,4-difluorophenoxy)benzoate

: 1609468-25-8
(S)-5-amino-3-(4-(2,4-difluorophenoxy)phenyl)-1-(piperidin-3-yl)-1H-pyrazole-4-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: water; sodium hydroxide / methanol / 3 h / 0 - 50 °C

2.1: thionyl chloride / Reflux

3.1: sodium hydride / tetrahydrofuran / 0.5 h / 0 °C / Inert atmosphere

3.2: 3 h / 20 °C

3.3: 18 h / Reflux

4.1: ethanol / 3 h / 20 °C

5.1: water; sodium hydroxide / ethanol / 24 h / 140 °C / Sealed tube

6.1: (ChiralPak OJ-H, / ethanol; isopropyl alcohol

With thionyl chloride; water; sodium hydride; sodium hydroxide; In tetrahydrofuran; methanol; ethanol; isopropyl alcohol;

Reference yield:

: 1609467-66-4
2-((4-(2,4-difluorophenoxy)phenyl)(methoxy)methylene)-malononitrile

: 1609468-25-8
(S)-5-amino-3-(4-(2,4-difluorophenoxy)phenyl)-1-(piperidin-3-yl)-1H-pyrazole-4-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / 3 h / 20 °C

2: water; sodium hydroxide / ethanol / 24 h / 140 °C / Sealed tube

3: (ChiralPak OJ-H, / ethanol; isopropyl alcohol

With water; sodium hydroxide; In ethanol; isopropyl alcohol;