4-(6-(4-(4-hydroxy-4-methylpiperidine-1-carbonyl)phenyl)imidazo[1,2-a]pyrazin-3-yl)benzonitrile

Base Information

Chemical Name:4-(6-(4-(4-hydroxy-4-methylpiperidine-1-carbonyl)phenyl)imidazo[1,2-a]pyrazin-3-yl)benzonitrile
CAS No.:1464150-51-3
Molecular Formula:C₂₆H₂₃N₅O₂
Molecular Weight:437.501
Hs Code.:

Synonyms:4-(6-(4-(4-hydroxy-4-methylpiperidine-1-carbonyl)phenyl)imidazo[1,2-a]pyrazin-3-yl)benzonitrile

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Chemical Property of 4-(6-(4-(4-hydroxy-4-methylpiperidine-1-carbonyl)phenyl)imidazo[1,2-a]pyrazin-3-yl)benzonitrile

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Technology Process of 4-(6-(4-(4-hydroxy-4-methylpiperidine-1-carbonyl)phenyl)imidazo[1,2-a]pyrazin-3-yl)benzonitrile

There total 5 articles about 4-(6-(4-(4-hydroxy-4-methylpiperidine-1-carbonyl)phenyl)imidazo[1,2-a]pyrazin-3-yl)benzonitrile 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: 57.0%

: 586375-35-1
4-methylpiperidin-4-ol hydrochloride

: 1464153-62-5
4-(3-(4-cyanophenyl)imidazo[1,2-a]pyrazin-6-yl)benzoic acid

: 1464150-51-3
4-(6-(4-(4-hydroxy-4-methylpiperidine-1-carbonyl)phenyl)imidazo[1,2-a]pyrazin-3-yl)benzonitrile

Guidance literature:: 4-(3-(4-cyanophenyl)imidazo[1,2-a]pyrazin-6-yl)benzoic acid; With 4-methyl-morpholine; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 1h; Inert atmosphere;

4-methylpiperidin-4-ol hydrochloride; In N,N-dimethyl-formamide; at 20 ℃; for 18h;

Reference yield:

: 1245644-42-1
6-bromo-3-iodo-imidazo[1,2-a]pyrazine

: 1464150-51-3
4-(6-(4-(4-hydroxy-4-methylpiperidine-1-carbonyl)phenyl)imidazo[1,2-a]pyrazin-3-yl)benzonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; potassium phosphate / water; N,N-dimethyl-formamide / 1 h / 90 °C

2.1: sodium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / water; N,N-dimethyl-formamide / 2 h / 90 °C / Inert atmosphere

3.1: water; lithium hydroxide monohydrate / methanol; tetrahydrofuran / 12 h / 20 °C

4.1: 4-methyl-morpholine; HATU / N,N-dimethyl-formamide / 1 h / 20 °C / Inert atmosphere

4.2: 18 h / 20 °C

With 4-methyl-morpholine; potassium phosphate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; lithium hydroxide monohydrate; water; sodium carbonate; HATU; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide;

Reference yield:

: 1464153-49-8
4-(6-bromoimidazo[1,2-a]pyrazin-3-vl)benzonitrile

: 1464150-51-3
4-(6-(4-(4-hydroxy-4-methylpiperidine-1-carbonyl)phenyl)imidazo[1,2-a]pyrazin-3-yl)benzonitrile

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium carbonate; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / water; N,N-dimethyl-formamide / 2 h / 90 °C / Inert atmosphere

2.1: water; lithium hydroxide monohydrate / methanol; tetrahydrofuran / 12 h / 20 °C

3.1: 4-methyl-morpholine; HATU / N,N-dimethyl-formamide / 1 h / 20 °C / Inert atmosphere

3.2: 18 h / 20 °C

With 4-methyl-morpholine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; lithium hydroxide monohydrate; water; sodium carbonate; HATU; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide;