(1S,4S,5R)-2-[(S)-1-phenylethyl]-4-(4-nitrobenzoyloxy)-2-azabicyclo[3.2.1]octane

Base Information

Chemical Name:(1S,4S,5R)-2-[(S)-1-phenylethyl]-4-(4-nitrobenzoyloxy)-2-azabicyclo[3.2.1]octane
CAS No.:1394910-36-1
Molecular Formula:C₂₂H₂₄N₂O₄
Molecular Weight:380.444
Hs Code.:

Synonyms:(1S,4S,5R)-2-[(S)-1-phenylethyl]-4-(4-nitrobenzoyloxy)-2-azabicyclo[3.2.1]octane

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Chemical Property of (1S,4S,5R)-2-[(S)-1-phenylethyl]-4-(4-nitrobenzoyloxy)-2-azabicyclo[3.2.1]octane

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Technology Process of (1S,4S,5R)-2-[(S)-1-phenylethyl]-4-(4-nitrobenzoyloxy)-2-azabicyclo[3.2.1]octane

There total 4 articles about (1S,4S,5R)-2-[(S)-1-phenylethyl]-4-(4-nitrobenzoyloxy)-2-azabicyclo[3.2.1]octane 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: 50.0%

: 215674-16-1
(1S,3R,4R)-2-[(S)-1-phenylethyl]-3-hydroxymethyl-2-azabicyclo[2.2.1]heptane

: 62-23-7
4-nitro-benzoic acid

: 1394910-36-1
(1S,4S,5R)-2-[(S)-1-phenylethyl]-4-(4-nitrobenzoyloxy)-2-azabicyclo[3.2.1]octane

Guidance literature:: With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 0 - 20 ℃; diastereospecific reaction; Inert atmosphere;
DOI:10.1016/j.tet.2012.07.028

Reference yield:

: 2627-86-3
(S)-1-phenyl-ethylamine

: 1394910-36-1
(1S,4S,5R)-2-[(S)-1-phenylethyl]-4-(4-nitrobenzoyloxy)-2-azabicyclo[3.2.1]octane

Guidance literature:: Multi-step reaction with 4 steps

2: palladium on activated charcoal; hydrogen; potassium carbonate

3: lithium aluminium tetrahydride

4: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

With lithium aluminium tetrahydride; palladium on activated charcoal; hydrogen; potassium carbonate; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; 1: Diels-Alder reaction;
DOI:10.1016/j.tet.2012.07.028

Reference yield:

: 223473-32-3
(1S,3R,4R)-2-<(1S)-phenylethyl>-2-aza-bicyclo<2.2.1>heptane-3-carboxylic acid ethyl ester

: 1394910-36-1
(1S,4S,5R)-2-[(S)-1-phenylethyl]-4-(4-nitrobenzoyloxy)-2-azabicyclo[3.2.1]octane

Guidance literature:: Multi-step reaction with 2 steps

1: lithium aluminium tetrahydride

2: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 0 - 20 °C / Inert atmosphere

With lithium aluminium tetrahydride; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran;
DOI:10.1016/j.tet.2012.07.028