Hydrochloric Acid → HCID 123608631, compound
Reaction equation
[CH2:1]([C@H:8]([NH:33]C(=O)OC(C)(C)C)[C@@H:9]([OH:32])[CH2:10][N:11]([CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)[NH:12][C:13](=[O:24])[C@@H:14]([NH:19][C:20]([O:22][CH3:23])=[O:21])[C:15]([CH3:18])([CH3:17])[CH3:16])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl>C1COCC1>[NH2:33][C@@H:8]([CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[C@@H:9]([OH:32])[CH2:10][N:11]([CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)[NH:12][C:13]([C@@H:14]([NH:19][C:20](=[O:21])[O:22][CH3:23])[C:15]([CH3:18])([CH3:17])[CH3:16])=[O:24]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 70 °C
Procedure
A solution of Example 5F in THF (4 mL) was treated with 4N HCl, and stirred at 70° C. for 3 hrs. The mixture was cooled to room temperature and quenched with saturated sodium bicarbonate and ethyl acetate. The organic layer was separated, washed with brine, dried over sodium sulfate, filtered and the solvents were evaporated to give 83 mg (100%) of the title compound.
Workup
- temperatureThe mixture was cooled to room temperature
- customquenched with saturated sodium bicarbonate and ethyl acetate
- customThe organic layer was separated
- washwashed with brine
- dry with materialdried over sodium sulfate
- filtrationfiltered
- customthe solvents were evaporated
Sources & evidence
- ORD record
- ord-51d6f924452e41ac81a0ec95cfce4330
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07696226B2
Reaction notes
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