7-[4-(1-aminocyclobutyl)-8-phenyl]-[1,2,4]triazole[4,3-a]-1,5-naphthyridin-1-ol

Base Information

Chemical Name:7-[4-(1-aminocyclobutyl)-8-phenyl]-[1,2,4]triazole[4,3-a]-1,5-naphthyridin-1-ol
CAS No.:1199555-32-2
Molecular Formula:C₂₅H₂₁N₅O
Molecular Weight:407.475
Hs Code.:

Synonyms:7-[4-(1-aminocyclobutyl)-8-phenyl]-[1,2,4]triazole[4,3-a]-1,5-naphthyridin-1-ol

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Chemical Property of 7-[4-(1-aminocyclobutyl)-8-phenyl]-[1,2,4]triazole[4,3-a]-1,5-naphthyridin-1-ol

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Technology Process of 7-[4-(1-aminocyclobutyl)-8-phenyl]-[1,2,4]triazole[4,3-a]-1,5-naphthyridin-1-ol

There total 7 articles about 7-[4-(1-aminocyclobutyl)-8-phenyl]-[1,2,4]triazole[4,3-a]-1,5-naphthyridin-1-ol 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:

: 1199556-63-2
tert-butyl {1-[4-(1-hydroxy-8-phenyl-[1,2,4]triazole[4,3-a]-1,5-naphthyridin-7-y)phenyl]cyclobutyl}carbamate

: 1199555-32-2
7-[4-(1-aminocyclobutyl)-8-phenyl]-[1,2,4]triazole[4,3-a]-1,5-naphthyridin-1-ol

Guidance literature:: With hydrazine; In 1,4-dioxane; at 80 ℃; for 0.0833333h; Microwave irradiation;

Reference yield:

: 1032349-96-4
tert-butyl [1-(4-chlorophenyl)cyclobutyl]carbamate

: 1199555-32-2
7-[4-(1-aminocyclobutyl)-8-phenyl]-[1,2,4]triazole[4,3-a]-1,5-naphthyridin-1-ol

Guidance literature:: Multi-step reaction with 6 steps

1.1: bis(tri-t-butylphosphine)palladium⁽⁰⁾ / 1,4-dioxane / 1.5 h / 100 °C / Inert atmosphere

2.1: isopropylmagnesium chloride / tetrahydrofuran / 0.25 h / -78 °C / Inert atmosphere

2.2: -78 - 0 °C

2.3: 0 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 80 - 120 °C / Inert atmosphere

4.1: hydrazine / 1,4-dioxane / 0.08 h / 100 °C / Microwave irradiation

5.1: 1,4-dioxane / 3 h / 100 °C / Inert atmosphere

6.1: hydrazine / 1,4-dioxane / 0.08 h / 80 °C / Microwave irradiation

With isopropylmagnesium chloride; potassium carbonate; hydrazine; bis(tri-t-butylphosphine)palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide;

Reference yield:

: 50921-39-6
1-(4-chlorophenyl)cyclobutane-1-carboxylic acid

: 1199555-32-2
7-[4-(1-aminocyclobutyl)-8-phenyl]-[1,2,4]triazole[4,3-a]-1,5-naphthyridin-1-ol

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium azide; tetrabutylammomium bromide; zinc trifluoromethanesulfonate / tetrahydrofuran / 18 h / 60 °C / Inert atmosphere

2.1: bis(tri-t-butylphosphine)palladium⁽⁰⁾ / 1,4-dioxane / 1.5 h / 100 °C / Inert atmosphere

3.1: isopropylmagnesium chloride / tetrahydrofuran / 0.25 h / -78 °C / Inert atmosphere

3.2: -78 - 0 °C

3.3: 0 °C

4.1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 80 - 120 °C / Inert atmosphere

5.1: hydrazine / 1,4-dioxane / 0.08 h / 100 °C / Microwave irradiation

6.1: 1,4-dioxane / 3 h / 100 °C / Inert atmosphere

7.1: hydrazine / 1,4-dioxane / 0.08 h / 80 °C / Microwave irradiation

With sodium azide; tetrabutylammomium bromide; isopropylmagnesium chloride; zinc trifluoromethanesulfonate; potassium carbonate; hydrazine; bis(tri-t-butylphosphine)palladium⁽⁰⁾; In tetrahydrofuran; 1,4-dioxane; N,N-dimethyl-formamide; 1.1: Curtius Rearrangement;