2-(1-(2-((3-isopropylisoxazol-5-yl)methylamino)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)benzonitrile

Base Information

Chemical Name:2-(1-(2-((3-isopropylisoxazol-5-yl)methylamino)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)benzonitrile
CAS No.:1394387-80-4
Molecular Formula:C₂₁H₂₆N₄O
Molecular Weight:350.464
Hs Code.:

Synonyms:2-(1-(2-((3-isopropylisoxazol-5-yl)methylamino)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)benzonitrile

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Chemical Property of 2-(1-(2-((3-isopropylisoxazol-5-yl)methylamino)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)benzonitrile

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Technology Process of 2-(1-(2-((3-isopropylisoxazol-5-yl)methylamino)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)benzonitrile

There total 7 articles about 2-(1-(2-((3-isopropylisoxazol-5-yl)methylamino)ethyl)-1,2,3,6-tetrahydropyridin-4-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:

: C₂₁H₂₄N₄O

: 1394387-80-4
2-(1-(2-((3-isopropylisoxazol-5-yl)methylamino)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)benzonitrile

Guidance literature:: With sodium tris(acetoxy)borohydride; at 20 ℃; for 2h;
DOI:10.1016/j.ejmech.2013.12.056

Reference yield:

: 79099-07-3
N-tert-butyloxycarbonylpiperidin-4-one

: 1394387-80-4
2-(1-(2-((3-isopropylisoxazol-5-yl)methylamino)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)benzonitrile

Guidance literature:: Multi-step reaction with 6 steps

1.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -78 °C

1.2: 2 h / 20 °C

1.3: 15 h / -78 - 20 °C

2.1: trifluoroacetic acid / dichloromethane / 5 h / 0 - 20 °C

3.1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 80 °C

4.1: hydrazine hydrate / ethanol / 2 h / 70 °C

5.1: dichloromethane / 2 h / Molecular sieve

6.1: sodium tris(acetoxy)borohydride / 2 h / 20 °C

With n-butyllithium; sodium tris(acetoxy)borohydride; potassium carbonate; hydrazine hydrate; trifluoroacetic acid; In tetrahydrofuran; ethanol; hexane; dichloromethane; N,N-dimethyl-formamide; 4.1: |Gabriel Amine Synthesis;
DOI:10.1016/j.ejmech.2013.12.056

Reference yield:

: 2-(1,2,3,6-tetrahydropyridin-4-yl)benzonitrile

: 1394387-80-4
2-(1-(2-((3-isopropylisoxazol-5-yl)methylamino)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)benzonitrile

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 80 °C

2: hydrazine hydrate / ethanol / 2 h / 70 °C

3: dichloromethane / 2 h / Molecular sieve

4: sodium tris(acetoxy)borohydride / 2 h / 20 °C

With sodium tris(acetoxy)borohydride; potassium carbonate; hydrazine hydrate; In ethanol; dichloromethane; N,N-dimethyl-formamide; 2: |Gabriel Amine Synthesis;
DOI:10.1016/j.ejmech.2013.12.056