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1240390-36-6

1240390-36-6 Structure

1240390-36-6 Structure
IdentificationBack Directory
[Name]

((3R,4R)-4-aMinotetrahydro-2H-pyran-3-yl)carbaMate
[CAS]

1240390-36-6
[Synonyms]

(3R,4R)-N3-Boc-tetrahydro-2H-pyran-3,4-diamine
((3R,4R)-4-aMinotetrahydro-2H-pyran-3-yl)carbaMate
tert-butyl N-[(3R,4R)-4-aminotetrahydropyran-3-yl]carbamate
tert-butyl ((3R,4R)-4-aMinotetrahydro-2H-pyran-3-yl)carbaMate
Carbamic acid, N-[(3R,4R)-4-aminotetrahydro-2H-pyran-3-yl]-, 1,1-dimethylethyl ester
[EINECS(EC#)]

604-604-1
[Molecular Formula]

C10H20N2O3
[MDL Number]

MFCD19105154
[MOL File]

1240390-36-6.mol
[Molecular Weight]

216.28
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[Appearance]

Colorless to light yellow Solid
Spectrum DetailBack Directory
[Spectrum Detail]

((3R,4R)-4-aMinotetrahydro-2H-pyran-3-yl)carbaMate(1240390-36-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

1,1-Dimethylethyl N-[(3R,4R)-4-azidotetrahydro-2H-pyran-3-yl]carbamate

1240390-35-5

((3R,4R)-4-aMinotetrahydro-2H-pyran-3-yl)carbaMate

1240390-36-6

Step 8: Tert-butyl (3R,4R)-4-azidotetrahydro-2H-pyran-3-ylcarbamate (700 mg, 2.89 mmol) was dissolved in ethanol (10 mL) and palladium/carbon hydroxide catalyst was added. The reaction was carried out under hydrogen (1 atm) atmosphere for 6 hours. After completion of the reaction, the palladium/carbon hydroxide was removed by filtration and the filtrate was concentrated to afford tert-butyl (3R,4R)-4-aminotetrahydro-2H-pyran-3-ylcarbamate (610 mg).

[References]

[1] Patent: WO2010/97248, 2010, A1. Location in patent: Page/Page column 38-39
[2] Patent: WO2013/78468, 2013, A1. Location in patent: Paragraph 0747; 0755
[3] Patent: US2017/15655, 2017, A1. Location in patent: Paragraph 1474-1475
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