1-(8-amino-1-(4-(4-(trifluoromethyl)pyridin-2-ylcarbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-N-isopropylpiperidine-3-carboxamide

Base Information

Chemical Name:1-(8-amino-1-(4-(4-(trifluoromethyl)pyridin-2-ylcarbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-N-isopropylpiperidine-3-carboxamide
CAS No.:1419216-30-0
Molecular Formula:C₂₈H₂₉F₃N₈O₂
Molecular Weight:566.586
Hs Code.:

Synonyms:1-(8-amino-1-(4-(4-(trifluoromethyl)pyridin-2-ylcarbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-N-isopropylpiperidine-3-carboxamide

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Chemical Property of 1-(8-amino-1-(4-(4-(trifluoromethyl)pyridin-2-ylcarbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-N-isopropylpiperidine-3-carboxamide

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Technology Process of 1-(8-amino-1-(4-(4-(trifluoromethyl)pyridin-2-ylcarbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-N-isopropylpiperidine-3-carboxamide

There total 9 articles about 1-(8-amino-1-(4-(4-(trifluoromethyl)pyridin-2-ylcarbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-N-isopropylpiperidine-3-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: 20.0%

: 1419222-78-8
1-(8-amino-1-(4-(4-(trifluoromethyl)pyridin-2-ylcarbamoyl)phenyl)-imidazo[1,5-a]pyrazin-3-yl)piperidine-3-carboxylic acid

: 75-31-0
isopropylamine

: 1419216-30-0
1-(8-amino-1-(4-(4-(trifluoromethyl)pyridin-2-ylcarbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-N-isopropylpiperidine-3-carboxamide

Guidance literature:: With triethylamine; HATU; In N,N-dimethyl-formamide; at 25 ℃; for 16h;

Reference yield:

: 1419222-76-6
methyl 1-(8-amino-1-bromoimidazo[1,5-a]pyrazin-3-yl)piperidine-3-carboxylate

: 1419216-30-0
1-(8-amino-1-(4-(4-(trifluoromethyl)pyridin-2-ylcarbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-N-isopropylpiperidine-3-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate / 1,4-dioxane / 2 h / 120 °C / Inert atmosphere

2: lithium hydroxide / water; tetrahydrofuran / 12 h / 20 °C

3: triethylamine; HATU / N,N-dimethyl-formamide / 16 h / 25 °C

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate; triethylamine; HATU; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; water; N,N-dimethyl-formamide;

Reference yield:

: 771581-15-8
(3-chloro-pyrazin-2-yl)-methylamine

: 1419216-30-0
1-(8-amino-1-(4-(4-(trifluoromethyl)pyridin-2-ylcarbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-N-isopropylpiperidine-3-carboxamide

Guidance literature:: Multi-step reaction with 8 steps

1.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 40 °C

1.2: 8 h / 40 °C

2.1: trichlorophosphate / acetonitrile / 3 h / 90 °C / Inert atmosphere

3.1: N-Bromosuccinimide / acetonitrile / 1 h / 20 °C

4.1: triethylamine / isopropyl alcohol / 16 h / 110 °C

5.1: trifluoroacetic acid / 12 h / 100 °C

6.1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium carbonate / 1,4-dioxane / 2 h / 120 °C / Inert atmosphere

7.1: lithium hydroxide / water; tetrahydrofuran / 12 h / 20 °C

8.1: triethylamine; HATU / N,N-dimethyl-formamide / 16 h / 25 °C

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; N-Bromosuccinimide; potassium carbonate; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; lithium hydroxide; trichlorophosphate; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; N,N-dimethyl-formamide; isopropyl alcohol; acetonitrile;