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

Synthesis

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