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

Base Information

Chemical Name:(1S,4R,5R)-2-[(S)-1-phenylethyl]-4-phenylsulfanyl-2-azabicyclo[3.2.1]octane
CAS No.:1394910-42-9
Molecular Formula:C₂₁H₂₅NS
Molecular Weight:323.502
Hs Code.:

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

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

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

There total 6 articles about (1S,4R,5R)-2-[(S)-1-phenylethyl]-4-phenylsulfanyl-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: 25.0%

: 1394910-37-2
(1S,4S,5R)-2-[(S)-1-phenylethyl]-4-chloro-2-azabicyclo[3.2.1]octane

: 930-69-8
sodium thiophenolate

: 1394910-42-9
(1S,4R,5R)-2-[(S)-1-phenylethyl]-4-phenylsulfanyl-2-azabicyclo[3.2.1]octane

Guidance literature:: In ethanol; at 20 ℃; for 24h;
DOI:10.1016/j.tet.2012.07.028

Reference yield:

: 223505-12-2
(1R,3R,4S)-2-<(1S)-phenylethyl>-2-aza-bicyclo<2.2.1>hept-5-ene-3-carboxylic acid ethyl ester

: 1394910-42-9
(1S,4R,5R)-2-[(S)-1-phenylethyl]-4-phenylsulfanyl-2-azabicyclo[3.2.1]octane

Guidance literature:: Multi-step reaction with 4 steps

1: palladium on activated charcoal; hydrogen; potassium carbonate

2: lithium aluminium tetrahydride

3: methanesulfonyl chloride; triethylamine / dichloromethane / 5 h / 0 °C

4: ethanol / 24 h / 20 °C

With lithium aluminium tetrahydride; palladium on activated charcoal; hydrogen; potassium carbonate; methanesulfonyl chloride; triethylamine; In ethanol; dichloromethane;
DOI:10.1016/j.tet.2012.07.028

Reference yield:

: 542-92-7,25568-84-7,7313-32-8
cyclopenta-1,3-diene

: 1394910-42-9
(1S,4R,5R)-2-[(S)-1-phenylethyl]-4-phenylsulfanyl-2-azabicyclo[3.2.1]octane

Guidance literature:: Multi-step reaction with 5 steps

2: palladium on activated charcoal; hydrogen; potassium carbonate

3: lithium aluminium tetrahydride

4: methanesulfonyl chloride; triethylamine / dichloromethane / 5 h / 0 °C

5: ethanol / 24 h / 20 °C

With lithium aluminium tetrahydride; palladium on activated charcoal; hydrogen; potassium carbonate; methanesulfonyl chloride; triethylamine; In ethanol; dichloromethane; 1: Diels-Alder reaction;
DOI:10.1016/j.tet.2012.07.028