N-cyclopropyl-4-(8-((tetrahydro-2H-pyran-4-yl)methylamino)imidazo[1,2-a]pyrazin-3-yl)benzamide

Base Information

Chemical Name:N-cyclopropyl-4-(8-((tetrahydro-2H-pyran-4-yl)methylamino)imidazo[1,2-a]pyrazin-3-yl)benzamide
CAS No.:1263420-63-8
Molecular Formula:C₂₂H₂₅N₅O₂
Molecular Weight:391.473
Hs Code.:

Synonyms:N-cyclopropyl-4-(8-((tetrahydro-2H-pyran-4-yl)methylamino)imidazo[1,2-a]pyrazin-3-yl)benzamide

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Chemical Property of N-cyclopropyl-4-(8-((tetrahydro-2H-pyran-4-yl)methylamino)imidazo[1,2-a]pyrazin-3-yl)benzamide

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Technology Process of N-cyclopropyl-4-(8-((tetrahydro-2H-pyran-4-yl)methylamino)imidazo[1,2-a]pyrazin-3-yl)benzamide

There total 8 articles about N-cyclopropyl-4-(8-((tetrahydro-2H-pyran-4-yl)methylamino)imidazo[1,2-a]pyrazin-3-yl)benzamide 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: 36.0%

: 130290-79-8
4-tetrahydropyranmethylamine

: 1263420-64-9
N-cyclopropyl-4-(8-(methylsulfonyl)imidazo[1,2-a]pyrazin-3-yl)benzamide

: 1263420-63-8
N-cyclopropyl-4-(8-((tetrahydro-2H-pyran-4-yl)methylamino)imidazo[1,2-a]pyrazin-3-yl)benzamide

Guidance literature:: In 1,4-dioxane; for 12h; Reflux;

Reference yield:

: 887475-39-0
3-bromo-8-methylsulfanyl-imidazo[1,2-a]pyrazine

: 1263420-63-8
N-cyclopropyl-4-(8-((tetrahydro-2H-pyran-4-yl)methylamino)imidazo[1,2-a]pyrazin-3-yl)benzamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 2 h / Reflux

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

2.2: pH 4

3.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 17 h / 20 °C

4.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 17 h / 20 °C

5.1: 1,4-dioxane / 12 h / Reflux

With water; sodium carbonate; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; HATU; lithium hydroxide; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 1263420-83-2
8-(methylthio)imidazo[1,2-a]pyrazine

: 1263420-63-8
N-cyclopropyl-4-(8-((tetrahydro-2H-pyran-4-yl)methylamino)imidazo[1,2-a]pyrazin-3-yl)benzamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium acetate; bromine; potassium bromide / methanol / 1 h / 0 °C

2.1: sodium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 2 h / Reflux

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

3.2: pH 4

4.1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 17 h / 20 °C

5.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 17 h / 20 °C

6.1: 1,4-dioxane / 12 h / Reflux

With water; bromine; sodium acetate; sodium carbonate; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; HATU; potassium bromide; lithium hydroxide; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide;