Hydrochloric Acid → HCID 69593507, compound
Reaction equation
C(OC(=O)[NH:7][C@H:8]([C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([CH2:17][N:18]2[CH2:23][CH2:22][O:21][CH2:20][CH2:19]2)[CH:12]=1)[CH2:9][OH:10])(C)(C)C.[ClH:25]>CO>[ClH:25].[NH2:7][C@H:8]([C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([CH2:17][N:18]2[CH2:23][CH2:22][O:21][CH2:20][CH2:19]2)[CH:12]=1)[CH2:9][OH:10]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
(R)-[2-Hydroxy-1-(3-morpholin-4-ylmethyl-phenyl)-ethyl]-carbamic acid tert-butyl ester (2.1 g, 6.25 mmol) in methanol (22 mL) was added hydrochloric acid (2.0M in ethyl ether) (10.88 mL, 21.8 mmol) and reaction mixture was stirred at room temperature for 5 hr. The reaction mixture was concentrated under vacuum to provide the title compound as a pale green solid (quantitative yield).
Workup
- concentrationThe reaction mixture was concentrated under vacuum
Sources & evidence
- ORD record
- ord-60310fcc01c542e6a20ea5ff3487eb86
- Source dataset
- uspto-grants-2006_05
- Patent number
- US07045551B2
Reaction notes
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