Hydrochloric Acid → HCID 67381404, compound
Reaction equation
[CH3:1][N:2]([CH3:21])[C:3]1[CH:4]=[CH:5][C:6]2[C:15]3[NH:14][CH2:13][CH2:12][CH2:11][C:10]=3[C:9](=[O:16])[N:8](COC)[C:7]=2[CH:20]=1.[ClH:22]>C(O)C>[ClH:22].[CH3:1][N:2]([CH3:21])[C:3]1[CH:4]=[CH:5][C:6]2[C:15]3[NH:14][CH2:13][CH2:12][CH2:11][C:10]=3[C:9](=[O:16])[NH:8][C:7]=2[CH:20]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
The compound (100 mg, 0.34 mmol) prepared in step 3 was dissolved in ethanol (5 ml) and added with conc. hydrochloric acid (1.0 ml). The mixture was stirred overnight at 80° C., cooled to room temperature, and concentrated under reduced pressure to obtain the title compound (89.6 mg, yield: 92%, yellow solid).
Workup
- temperaturecooled to room temperature
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-2dfb274999c048f090da80b96dfd2f3c
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08815891B2
Reaction notes
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