Hydrochloric Acid → HCID 67381332, compound
Reaction equation
[CH3:1][N:2]([CH3:23])[CH2:3][CH2:4][C:5]1[CH:22]=[CH:21][C:8]2[N:9](COC)[C:10](=[O:17])[C:11]3[CH2:12][CH2:13][CH2:14][NH:15][C:16]=3[C:7]=2[CH:6]=1.[ClH:24]>C(O)C>[ClH:24].[ClH:24].[CH3:23][N:2]([CH3:1])[CH2:3][CH2:4][C:5]1[CH:22]=[CH:21][C:8]2[NH:9][C:10](=[O:17])[C:11]3[CH2:12][CH2:13][CH2:14][NH:15][C:16]=3[C:7]=2[CH:6]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
The compound (20 mg, 0.06 mmol) prepared in step 7 was dissolved in ethanol (4 ml) and added with conc. hydrochloric acid (0.5 ml). The resulting mixture was stirred for 8 hours at 80° C. and cooled to room temperature. The mixture was then concentrated under reduced pressure to obtain the title compound (18 mg, yield: 82%, yellow solid).
Workup
- temperaturecooled to room temperature
- concentrationThe mixture was then concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-6b04e977c3cf41a3b622d6479f339fcf
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08815891B2
Reaction notes
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