(7-(5-chlorobenzo[d]oxazol-2-yl)-3,7-diazabicyclo[3.3.1]nonan-3-yl)(5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone

Base Information

Chemical Name:(7-(5-chlorobenzo[d]oxazol-2-yl)-3,7-diazabicyclo[3.3.1]nonan-3-yl)(5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone
CAS No.:1429773-09-0
Molecular Formula:C₂₄H₂₃ClN₆O₂
Molecular Weight:462.939
Hs Code.:

Synonyms:(7-(5-chlorobenzo[d]oxazol-2-yl)-3,7-diazabicyclo[3.3.1]nonan-3-yl)(5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone

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Chemical Property of (7-(5-chlorobenzo[d]oxazol-2-yl)-3,7-diazabicyclo[3.3.1]nonan-3-yl)(5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone

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Technology Process of (7-(5-chlorobenzo[d]oxazol-2-yl)-3,7-diazabicyclo[3.3.1]nonan-3-yl)(5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone

There total 6 articles about (7-(5-chlorobenzo[d]oxazol-2-yl)-3,7-diazabicyclo[3.3.1]nonan-3-yl)(5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone 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:

: 3621-81-6
2,5-dichloro-1,3-benzoxazole

: 3,7-diazabicyclo[3.3.1]nonan-3-yl(5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl)-methanone?hydrochloride

: 1429773-09-0
(7-(5-chlorobenzo[d]oxazol-2-yl)-3,7-diazabicyclo[3.3.1]nonan-3-yl)(5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone

Guidance literature:: With potassium carbonate; In o-xylene; for 0.5h; Reflux;

Reference yield:

: 227940-71-8
tert-Butyl 7-benzyl-3,7-diazabicyclo[3.3. 1]-nonane-3-carboxylate

: 1429773-09-0
(7-(5-chlorobenzo[d]oxazol-2-yl)-3,7-diazabicyclo[3.3.1]nonan-3-yl)(5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogen; palladium 10% on activated carbon / water; ethanol / 16 h / 20 °C / 760.05 Torr

2: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / acetonitrile / 1 h / 20 °C

3: hydrogenchloride / 2 h / 20 °C

4: potassium carbonate / o-xylene / 0.5 h / Reflux

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; potassium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In ethanol; o-xylene; water; acetonitrile;

Reference yield:

: 227940-70-7
7-benzyl-9-oxo-3,7-diazabicyclo[3.3.1]nonane-3-carboxylic acid tert-butyl ester

: 1429773-09-0
(7-(5-chlorobenzo[d]oxazol-2-yl)-3,7-diazabicyclo[3.3.1]nonan-3-yl)(5-methyl-2-(2H-1,2,3-triazol-2-yl)phenyl)methanone

Guidance literature:: Multi-step reaction with 6 steps

1: ethanol / 1 h / 95 °C

2: sodium tetrahydroborate; water / tetrahydrofuran / 0 - 20 °C / Reflux

3: hydrogen; palladium 10% on activated carbon / water; ethanol / 16 h / 20 °C / 760.05 Torr

4: O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / acetonitrile / 1 h / 20 °C

5: hydrogenchloride / 2 h / 20 °C

6: potassium carbonate / o-xylene / 0.5 h / Reflux

With hydrogenchloride; sodium tetrahydroborate; palladium 10% on activated carbon; water; hydrogen; potassium carbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; o-xylene; water; acetonitrile;