Hydrochloric Acid → HCID 69038784, compound
Reaction equation
[CH2:1]([O:3][C:4]([N:6]1[CH2:11][CH2:10][C:9]([CH2:20][CH2:21][NH2:22])([NH:12]C(OC(C)(C)C)=O)[CH2:8][CH2:7]1)=[O:5])[CH3:2].[ClH:23].C(OCC)C>C(O)(C)C>[ClH:23].[CH2:1]([O:3][C:4]([N:6]1[CH2:11][CH2:10][C:9]([NH2:12])([CH2:20][CH2:21][NH2:22])[CH2:8][CH2:7]1)=[O:5])[CH3:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 3.01 g (9.56 mmol) of 4-(2-amino-ethyl)-4-tert-butoxycarbonylamino-piperidine-1-carboxylic acid ethyl ester in 19 ml of isopropanol was added 8 ml of a solution of hydrochloric acid (5.6 N) in isopropanol and the resulting solution was stirred at room temperature for 3 h. The mixture was cooled and diethyl ether was added. The resulting precipitate was filtered. The product was dried to give 2.49 g of pure compound as a white solid.
Workup
- temperatureThe mixture was cooled
- filtrationThe resulting precipitate was filtered
- customThe product was dried
Sources & evidence
- ORD record
- ord-85efd189b98a4ee891efc72279fde7d6
- Source dataset
- uspto-grants-2007_11
- Patent number
- US07294631B2
Reaction notes
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