Hydrochloric Acid → HCID 67410395, compound
Reaction equation
[CH3:1][N:2]([CH3:24])[CH2:3][CH2:4][O:5][C:6]1[CH:23]=[CH:22][C:9]2[N:10](COC)[C:11](=[O:18])[C:12]3[CH2:13][CH2:14][CH2:15][NH:16][C:17]=3[C:8]=2[CH:7]=1.[ClH:25]>C(O)C>[ClH:25].[CH3:1][N:2]([CH3:24])[CH2:3][CH2:4][O:5][C:6]1[CH:23]=[CH:22][C:9]2[NH:10][C:11](=[O:18])[C:12]3[CH2:13][CH2:14][CH2:15][NH:16][C:17]=3[C:8]=2[CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 90 °C
Procedure
The compound (40 mg, 0.120 mmol) prepared in step 7 was dissolved in ethanol (3 ml), added with 12 N hydrochloric acid (2 ml). The resulting mixture was refluxed for 12 hours at 90° C. Once the reaction was completed, the mixture was concentrated under reduced pressure and the residue was washed ethyl acetate to obtain the title compound (36 mg, yield: 84%, yellow solid).
Workup
- concentrationthe mixture was concentrated under reduced pressure
- washthe residue was washed ethyl acetate
Sources & evidence
- ORD record
- ord-d365572a105543f0a265bcbd813e291e
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08815891B2
Reaction notes
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