Hydrochloric Acid → HCID 117770605, compound
Reaction equation
C(OC(=O)[NH:7][CH2:8][CH2:9][O:10][C:11]1[CH:12]=[N:13][C:14]([Br:17])=[CH:15][CH:16]=1)(C)(C)C.[ClH:19]>C(O)C.C(OCC)(=O)C>[ClH:19].[ClH:19].[Br:17][C:14]1[N:13]=[CH:12][C:11]([O:10][CH2:9][CH2:8][NH2:7])=[CH:16][CH:15]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of tert-butyl(2-((6-bromopyridin-3-yl)oxy)ethyl)carbamate obtained in Reference Example 4 (1.20 g) in ethanol (25 mL) was added a 4M solution of hydrogen chloride in ethyl acetate (10 mL) at room temperature. The mixture was stirred at room temperature for 3 days, and the solvent was evaporated under reduced pressure. To the residue was added ethanol, the solvent was evaporated under reduced pressure, and the precipitated solid was collected by filtration to give the title compound (1.09 g).
Workup
- customthe solvent was evaporated under reduced pressure
- additionTo the residue was added ethanol
- customthe solvent was evaporated under reduced pressure
- filtrationthe precipitated solid was collected by filtration
Sources & evidence
- ORD record
- ord-b3a858d5a1394a43b1ff9c262ecb0a5a
- Source dataset
- uspto-grants-2015_07
- Patent number
- US09085578B2
Reaction notes
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