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17366-48-2

17366-48-2 Structure

17366-48-2 Structure
IdentificationBack Directory
[Name]

Exo-3-hydroxy-8-azabicyclo[3.2.1]octane hydrochloride
[CAS]

17366-48-2
[Synonyms]

Exo-3-hydroxy-8-azabicycl...
EXO-3-HYDROXY-8-AZABICYCLO[3.2.1]OCTANE HCL
exo-8-Azabicyclo[3.2.1]octan-3-ol hydrochloride
(3-exo)-8-Azabicyclo[3.2.1]octan-3-ol hydrochloride
Exo-3-hydroxy-8-azabicyclo[3.2.1]octane hydrochloride
8-Azabicyclo[3.2.1]octan-3-ol, hydrochloride (1:1), (3-exo)-
[Molecular Formula]

C7H14ClNO
[MDL Number]

MFCD21642368
[MOL File]

17366-48-2.mol
[Molecular Weight]

163.645
Chemical PropertiesBack Directory
[Melting point ]

200 °C
[storage temp. ]

Inert atmosphere,Room Temperature
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

Exo-3-hydroxy-8-azabicyclo[3.2.1]octane hydrochloride(17366-48-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-exo-Hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester

194222-05-4

Exo-3-hydroxy-8-azabicyclo[3.2.1]octane hydrochloride

17366-48-2

Step 1. Preparation of (1R,3S,5S)-8-azabicyclo[3.2.1]octan-3-ol hydrochloride: tert-butyl (1R,3S,5S)-3-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate (300 mg, 1.32 mmol) was dissolved in a solution of 1,4-dioxane (4.0 mL) in 4 M HCl and the reaction was stirred at room temperature for 15 hours. After completion of the reaction, the mixture was concentrated under reduced pressure to give the target product (168 mg, quantitative yield) as a white solid, which could be used in subsequent steps without further purification.LC-MS analysis: calculated value 127.1 [M + H]+, measured value 127.90 [M + H]+.

[References]

[1] Patent: US2012/53180, 2012, A1. Location in patent: Page/Page column 35
[2] Patent: WO2013/61305, 2013, A1. Location in patent: Page/Page column 44
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