(3R,5R,7R)-N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-((2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)methyl)benzyl)adamantane-1-carboxamide

Base Information

Chemical Name:(3R,5R,7R)-N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-((2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)methyl)benzyl)adamantane-1-carboxamide
CAS No.:1404098-46-9
Molecular Formula:C₃₄H₃₆N₆O₄
Molecular Weight:592.698
Hs Code.:

(3R,5R,7R)-N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-((2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)methyl)benzyl)adamantane-1-carboxamide

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Chemical Property of (3R,5R,7R)-N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-((2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)methyl)benzyl)adamantane-1-carboxamide

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Technology Process of (3R,5R,7R)-N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-((2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)methyl)benzyl)adamantane-1-carboxamide

There total 6 articles about (3R,5R,7R)-N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-((2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)methyl)benzyl)adamantane-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: 39.2%

: 67-52-7,944357-77-1
BARBITURIC ACID

: 1404097-74-0
(3r,5r,7r)-N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-formylbenzyl)adamantane-1-carboxamide

: 1404098-46-9
(3R,5R,7R)-N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-((2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)methyl)benzyl)adamantane-1-carboxamide

Guidance literature:: In ethanol; water; at 80 ℃; Reflux;
DOI:10.1021/jm301164y

Reference yield:

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

: 1404098-46-9
(3R,5R,7R)-N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-((2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)methyl)benzyl)adamantane-1-carboxamide

Guidance literature:: Multi-step reaction with 7 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

7: ethanol; water / 80 °C / Reflux

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

Reference yield:

: C₂₃H₂₈N₄O₂

: 1404098-46-9
(3R,5R,7R)-N-(1-(3-cyanopyridin-2-yl)piperidin-4-yl)-N-(4-((2,4,6-trioxotetrahydropyrimidin-5(2H)-ylidene)methyl)benzyl)adamantane-1-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

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

2: hydrogenchloride / water; acetone / 0.5 h

3: triethylamine / dichloromethane / 20 - 25 °C

4: ethanol; water / 80 °C / Reflux

With hydrogenchloride; sodium tetrahydroborate; triethylamine; In methanol; ethanol; dichloromethane; water; acetone;
DOI:10.1021/jm301164y