(1R,2R,3R,5S)-3-(4-Fluoro-phenyl)-8-methyl-2-(3-methyl-[1,2,4]oxadiazol-5-yl)-8-aza-bicyclo[3.2.1]octane

Base Information

Chemical Name:(1R,2R,3R,5S)-3-(4-Fluoro-phenyl)-8-methyl-2-(3-methyl-[1,2,4]oxadiazol-5-yl)-8-aza-bicyclo[3.2.1]octane
CAS No.:184376-51-0
Molecular Formula:C₁₇H₂₀FN₃O
Molecular Weight:301.364
Hs Code.:

Synonyms:(1R,2R,3R,5S)-3-(4-Fluoro-phenyl)-8-methyl-2-(3-methyl-[1,2,4]oxadiazol-5-yl)-8-aza-bicyclo[3.2.1]octane

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Chemical Property of (1R,2R,3R,5S)-3-(4-Fluoro-phenyl)-8-methyl-2-(3-methyl-[1,2,4]oxadiazol-5-yl)-8-aza-bicyclo[3.2.1]octane

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Technology Process of (1R,2R,3R,5S)-3-(4-Fluoro-phenyl)-8-methyl-2-(3-methyl-[1,2,4]oxadiazol-5-yl)-8-aza-bicyclo[3.2.1]octane

There total 1 articles about (1R,2R,3R,5S)-3-(4-Fluoro-phenyl)-8-methyl-2-(3-methyl-[1,2,4]oxadiazol-5-yl)-8-aza-bicyclo[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: 85.0%

: 1493-23-8
(4-fluorophenyl)lithium

: (1R,5S)-2-(3'-methyl-1',2',4'-oxadiazol-5'-yl)-8-methyl-8-azabicyclo[3.2.1]oct-2-ene

: 184376-51-0
(1R,2R,3R,5S)-3-(4-Fluoro-phenyl)-8-methyl-2-(3-methyl-[1,2,4]oxadiazol-5-yl)-8-aza-bicyclo[3.2.1]octane

Guidance literature:: In tetrahydrofuran; at -78 ℃;
DOI:10.1021/jm960515u

Reference yield:

: 184376-51-0
(1R,2R,3R,5S)-3-(4-Fluoro-phenyl)-8-methyl-2-(3-methyl-[1,2,4]oxadiazol-5-yl)-8-aza-bicyclo[3.2.1]octane

: 201472-82-4
[(1R,2S,3R,5S)-3-(4-Fluoro-phenyl)-8-methyl-8-aza-bicyclo[3.2.1]oct-2-yl]-methanol

Guidance literature:: Multi-step reaction with 2 steps

1: 1.03 g / Ni₂B, 12N aq. HCl / a) RT, 2 h, b) reflux, 3 h

2: LiAlH₄ / diethyl ether / 2 h / Ambient temperature

With hydrogenchloride; lithium aluminium tetrahydride; nickel boride; In diethyl ether;
DOI:10.1021/jm970669p

Reference yield:

: 184376-51-0
(1R,2R,3R,5S)-3-(4-Fluoro-phenyl)-8-methyl-2-(3-methyl-[1,2,4]oxadiazol-5-yl)-8-aza-bicyclo[3.2.1]octane

: Methanesulfonic acid (1R,2S,3R,5S)-3-(4-fluoro-phenyl)-8-methyl-8-aza-bicyclo[3.2.1]oct-2-ylmethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1.03 g / Ni₂B, 12N aq. HCl / a) RT, 2 h, b) reflux, 3 h

2: LiAlH₄ / diethyl ether / 2 h / Ambient temperature

3: Et₃N / CH₂Cl₂ / 3.5 h / 0 - 20 °C

With hydrogenchloride; lithium aluminium tetrahydride; nickel boride; triethylamine; In diethyl ether; dichloromethane;
DOI:10.1021/jm970669p