(2S,5R)-5-(8-amino-1-(4-((4-(trifluoromethyl)pyridin-2-yl)carbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-2-(hydroxymethyl)-N-methylpiperidine-1-carboxamide

Base Information

Chemical Name:(2S,5R)-5-(8-amino-1-(4-((4-(trifluoromethyl)pyridin-2-yl)carbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-2-(hydroxymethyl)-N-methylpiperidine-1-carboxamide
CAS No.:1620678-30-9
Molecular Formula:C₂₇H₂₇F₃N₈O₃
Molecular Weight:568.558
Hs Code.:

(2S,5R)-5-(8-amino-1-(4-((4-(trifluoromethyl)pyridin-2-yl)carbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-2-(hydroxymethyl)-N-methylpiperidine-1-carboxamide

Synonyms:(2S,5R)-5-(8-amino-1-(4-((4-(trifluoromethyl)pyridin-2-yl)carbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-2-(hydroxymethyl)-N-methylpiperidine-1-carboxamide

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Chemical Property of (2S,5R)-5-(8-amino-1-(4-((4-(trifluoromethyl)pyridin-2-yl)carbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-2-(hydroxymethyl)-N-methylpiperidine-1-carboxamide

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Technology Process of (2S,5R)-5-(8-amino-1-(4-((4-(trifluoromethyl)pyridin-2-yl)carbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-2-(hydroxymethyl)-N-methylpiperidine-1-carboxamide

There total 8 articles about (2S,5R)-5-(8-amino-1-(4-((4-(trifluoromethyl)pyridin-2-yl)carbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-2-(hydroxymethyl)-N-methylpiperidine-1-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: 15.0%

: 1620678-29-6
4-(8-amino-3-((3R,6S)-6-(hydroxymethyl)piperidin-3-yl)imidazo[1,5-a]pyrazin-1-yl)-N-(4-(trifluoromethyl)pyridin-2-yl)benzamide

: 6452-47-7
methylcarbamoyl chloride

: 1620678-30-9
(2S,5R)-5-(8-amino-1-(4-((4-(trifluoromethyl)pyridin-2-yl)carbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-2-(hydroxymethyl)-N-methylpiperidine-1-carboxamide

Guidance literature:: With triethylamine; In tetrahydrofuran; at 0 - 20 ℃; for 3h;

Reference yield:

: 1620678-28-5
(2S,5R)-benzyl 5-(8-amino-1-(4-((4-(trifluoromethyl)pyridin-2-yl)carbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-2-(methoxymethyl)piperidine-1-carboxylate

: 1620678-30-9
(2S,5R)-5-(8-amino-1-(4-((4-(trifluoromethyl)pyridin-2-yl)carbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-2-(hydroxymethyl)-N-methylpiperidine-1-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: boron tribromide / dichloromethane / 7 h / -78 °C

1.2: -78 °C

2.1: triethylamine / tetrahydrofuran / 3 h / 0 - 20 °C

With boron tribromide; triethylamine; In tetrahydrofuran; dichloromethane;

Reference yield:

: 1620675-76-4
(2S,5R)-benzyl 5-(8-chloroimidazo[1,5-a]pyrazin-3-yl)-2-(methoxymethyl)piperidine-1-carboxylate

: 1620678-30-9
(2S,5R)-5-(8-amino-1-(4-((4-(trifluoromethyl)pyridin-2-yl)carbamoyl)phenyl)imidazo[1,5-a]pyrazin-3-yl)-2-(hydroxymethyl)-N-methylpiperidine-1-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

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

2.1: ammonium hydroxide / isopropyl alcohol / 7 h / 100 °C / Sealed tube

3.1: potassium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / water; 1,4-dioxane / 1 h / 100 °C / Inert atmosphere

4.1: boron tribromide / dichloromethane / 7 h / -78 °C

4.2: -78 °C

5.1: triethylamine / tetrahydrofuran / 3 h / 0 - 20 °C

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; ammonium hydroxide; N-Bromosuccinimide; boron tribromide; potassium carbonate; triethylamine; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; isopropyl alcohol; acetonitrile;