Hydrochloric Acid → 1609345-55-2
Reaction equation
[ClH:1].C(OCC)C.[F:7][C:8]1([F:24])[CH2:13][CH2:12][N:11]([CH2:14][CH2:15][NH:16]C(=O)OC(C)(C)C)[CH2:10][CH2:9]1>>[ClH:1].[ClH:1].[F:24][C:8]1([F:7])[CH2:9][CH2:10][N:11]([CH2:14][CH2:15][NH2:16])[CH2:12][CH2:13]1Participants
4
Procedure
6.9 ml of a 2 N solution of hydrogen chloride in diethyl ether (13.8 mmol, 10 equivalents) were added to 500 mg of tert-butyl [2-(4,4-difluoropiperidin-1-yl)ethyl]carbamate (Example 166A, 1.38 mmol, 1 equivalent), and the mixture was stirred at RT overnight. The solvent was decanted off, the residue was triturated three times with diethyl ether, the diethyl ether was decanted off and the product obtained in this manner was dried under reduced pressure. This gave 448 mg (100% of theory; purity 73%) of the title compound.
Workup
- customThe solvent was decanted off
- customthe residue was triturated three times with diethyl ether
- customthe diethyl ether was decanted off
- customthe product obtained in this manner
- customwas dried under reduced pressure
Sources & evidence
- ORD record
- ord-46cff41c013844bbbb50f827e2a10450
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09126998B2
Reaction notes
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