(-)-dimethyl-[5-(8-trityl-8-azabicyclo[3.2.1]oct-6-yl)pyridine-2-yl]amine

Base Information

Chemical Name:(-)-dimethyl-[5-(8-trityl-8-azabicyclo[3.2.1]oct-6-yl)pyridine-2-yl]amine
CAS No.:1421915-96-9
Molecular Formula:C₃₃H₃₅N₃
Molecular Weight:473.661
Hs Code.:

Synonyms:(-)-dimethyl-[5-(8-trityl-8-azabicyclo[3.2.1]oct-6-yl)pyridine-2-yl]amine

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Chemical Property of (-)-dimethyl-[5-(8-trityl-8-azabicyclo[3.2.1]oct-6-yl)pyridine-2-yl]amine

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Technology Process of (-)-dimethyl-[5-(8-trityl-8-azabicyclo[3.2.1]oct-6-yl)pyridine-2-yl]amine

There total 7 articles about (-)-dimethyl-[5-(8-trityl-8-azabicyclo[3.2.1]oct-6-yl)pyridine-2-yl]amine 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: 35.0%

: 1421915-92-5
(-)-(1R,5S,6S)-6-(6-dimethylamino-pyridine-3-yl)-8-azabicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester

: 76-83-5
trityl chloride

: 1421915-96-9
(-)-dimethyl-[5-(8-trityl-8-azabicyclo[3.2.1]oct-6-yl)pyridine-2-yl]amine

Guidance literature:: With triethylamine; In chloroform; at 20 ℃; for 7.5h;

Reference yield:

: 845642-53-7
(-)-(1R,5S,6S)-6-(6-fluoro-pyridine-3-yl)-8-azabicyclo[3.2.1]octane

: 1421915-96-9
(-)-dimethyl-[5-(8-trityl-8-azabicyclo[3.2.1]oct-6-yl)pyridine-2-yl]amine

Guidance literature:: Multi-step reaction with 3 steps

1: ethanol / 23 h / 100 °C / Autoclave

2: triethylamine / tetrahydrofuran / 4 h / 20 °C

3: triethylamine / chloroform / 7.5 h / 20 °C

With triethylamine; In tetrahydrofuran; ethanol; chloroform;

Reference yield:

: 171197-80-1
2-fluoro-5-iodopyridine

: 1421915-96-9
(-)-dimethyl-[5-(8-trityl-8-azabicyclo[3.2.1]oct-6-yl)pyridine-2-yl]amine

Guidance literature:: Multi-step reaction with 6 steps

1: trans-di(μ-acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II); triethylamine; formic acid / N,N-dimethyl-formamide / 4 h / 70 °C / Inert atmosphere

2: cyclohexene; palladium 10% on activated carbon / ethanol / 19 h / Inert atmosphere; Reflux

3: CHIRALPAK? IA column / diethylamine; acetonitrile / Resolution of racemate

4: ethanol / 23 h / 100 °C / Autoclave

5: triethylamine / tetrahydrofuran / 4 h / 20 °C

6: triethylamine / chloroform / 7.5 h / 20 °C

With formic acid; trans-di(μ-acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II); palladium 10% on activated carbon; triethylamine; cyclohexene; In tetrahydrofuran; ethanol; chloroform; diethylamine; N,N-dimethyl-formamide; acetonitrile;