N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-formylbenzyl)pentanamide

Base Information

Chemical Name:N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-formylbenzyl)pentanamide
CAS No.:1404097-76-2
Molecular Formula:C₂₄H₂₈N₄O₂
Molecular Weight:404.512
Hs Code.:

Synonyms:N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-formylbenzyl)pentanamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-formylbenzyl)pentanamide

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Technology Process of N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-formylbenzyl)pentanamide

There total 5 articles about N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-formylbenzyl)pentanamide 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: 61.4%

: 1404097-65-9
2-(4-((4-formylbenzyl)amino)piperidin-1-yl)nicotinonitrile

: 638-29-9
n-valeryl chloride

: 1404097-76-2
N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-formylbenzyl)pentanamide

Guidance literature:: With triethylamine; In dichloromethane; at 20 - 25 ℃;
DOI:10.1021/jm301164y

Reference yield:

: 6602-54-6
2-chloro-3-pyridinecarbonitrile

: 1404097-76-2
N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-formylbenzyl)pentanamide

Guidance literature:: Multi-step reaction with 6 steps

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

2: dichloromethane / 3 h / 0 - 25 °C

3: potassium carbonate / ethanol; water / 25 - 80 °C

4: sodium tetrahydroborate / methanol / 0.5 h / 0 - 60 °C

5: hydrogenchloride / water; acetone / 0.5 h

6: triethylamine / dichloromethane / 20 - 25 °C

With hydrogenchloride; sodium tetrahydroborate; potassium carbonate; triethylamine; In methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm301164y

Reference yield:

: 73874-95-0
(piperidin-4-yl)carbamic acid tert-butyl ester

: 1404097-76-2
N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-formylbenzyl)pentanamide

Guidance literature:: Multi-step reaction with 6 steps

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

2: dichloromethane / 3 h / 0 - 25 °C

3: potassium carbonate / ethanol; water / 25 - 80 °C

4: sodium tetrahydroborate / methanol / 0.5 h / 0 - 60 °C

5: hydrogenchloride / water; acetone / 0.5 h

6: triethylamine / dichloromethane / 20 - 25 °C

With hydrogenchloride; sodium tetrahydroborate; potassium carbonate; triethylamine; In methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm301164y