(3-((3-amino-4-(4-phenoxyphenyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)amino)-1H-pyrazol-1-yl)acetic acid

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Chemical Name:(3-((3-amino-4-(4-phenoxyphenyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)amino)-1H-pyrazol-1-yl)acetic acid
CAS No.:1266160-43-3
Molecular Formula:C₂₃H₁₉N₇O₃
Molecular Weight:441.449
Hs Code.:

Synonyms:(3-((3-amino-4-(4-phenoxyphenyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)amino)-1H-pyrazol-1-yl)acetic acid

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Chemical Property of (3-((3-amino-4-(4-phenoxyphenyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)amino)-1H-pyrazol-1-yl)acetic acid

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Technology Process of (3-((3-amino-4-(4-phenoxyphenyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)amino)-1H-pyrazol-1-yl)acetic acid

There total 6 articles about (3-((3-amino-4-(4-phenoxyphenyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)amino)-1H-pyrazol-1-yl)acetic acid 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:

: 1266162-08-6
2-(3-(4-chloro-5-cyano-6-(4-phenoxyphenyl)pyridin-2-ylamino)-1H-pyrazol-1-yl)acetic acid

: 1266160-43-3
(3-((3-amino-4-(4-phenoxyphenyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)amino)-1H-pyrazol-1-yl)acetic acid

Guidance literature:: With hydrazine; In ISOPROPYLAMIDE; at 100 ℃; for 3h;

Reference yield:

: 3096-81-9
4-phenoxybenzonitrile

: 1266160-43-3
(3-((3-amino-4-(4-phenoxyphenyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)amino)-1H-pyrazol-1-yl)acetic acid

Guidance literature:: Multi-step reaction with 6 steps

1: N-ethyl-N,N-diisopropylamine; n-butyllithium / tetrahydrofuran / 2 h / -78 °C

2: 0.17 h / 250 °C / Microwave irradiation

3: trichlorophosphate / 2 h / 90 °C / Sonographic reaction

4: caesium carbonate / 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere; Sealed tube

5: sodium hydroxide; water / dimethyl sulfoxide; methanol / 1 h / 20 °C

6: hydrazine / ISOPROPYLAMIDE / 3 h / 100 °C

With n-butyllithium; water; caesium carbonate; N-ethyl-N,N-diisopropylamine; sodium hydroxide; hydrazine; trichlorophosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In tetrahydrofuran; 1,4-dioxane; methanol; ISOPROPYLAMIDE; dimethyl sulfoxide;

Reference yield:

: 1266161-61-8
3-amino-3-(4-phenoxyphenyl)acrylonitrile

: 1266160-43-3
(3-((3-amino-4-(4-phenoxyphenyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)amino)-1H-pyrazol-1-yl)acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1: 0.17 h / 250 °C / Microwave irradiation

2: trichlorophosphate / 2 h / 90 °C / Sonographic reaction

3: caesium carbonate / 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane / 16 h / 80 °C / Inert atmosphere; Sealed tube

4: sodium hydroxide; water / dimethyl sulfoxide; methanol / 1 h / 20 °C

5: hydrazine / ISOPROPYLAMIDE / 3 h / 100 °C

With water; caesium carbonate; sodium hydroxide; hydrazine; trichlorophosphate; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; methanol; ISOPROPYLAMIDE; dimethyl sulfoxide;