Hydrochloric Acid → HCID 71226271, compound
Reaction equation
[CH3:1][C:2]1[N:3]([C@H:8]2[CH2:15][C@@:14]3([C:16]([O:18]C)=[O:17])[C@H:10]([CH2:11][CH2:12][CH2:13]3)[CH2:9]2)[C:4]([CH3:7])=[CH:5][CH:6]=1.[OH-].[Na+].Cl>CO.O>[CH3:1][C:2]1[N:3]([C@H:8]2[CH2:15][C@@:14]3([C:16]([OH:18])=[O:17])[C@H:10]([CH2:11][CH2:12][CH2:13]3)[CH2:9]2)[C:4]([CH3:7])=[CH:5][CH:6]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 65 °C
Procedure
To a solution of Example 1D (5.3 g, 20.3 mmol) in methanol (33 mL) and water (15 mL) was added a aqueous solution of sodium hydroxide (3.2 g, 80 mmol in 4 mL of water) and the mixture was heated at 65° C. for 16 hours. The mixture was cooled to room temperature, acidified to pH=4 with 4N hydrochloric acid. The solid was filtered to afford Example 1E which was used in next step without further purification.
Workup
- temperatureThe mixture was cooled to room temperature
- filtrationThe solid was filtered
- customto afford Example 1E which
- customwas used in next step without further purification
Sources & evidence
- ORD record
- ord-1970057ccb114405994b4a4a3c75dc48
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08906911B2
Reaction notes
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