Hydrochloric Acid → HCID 178479655, compound
Reaction equation
[NH:1]1[C:5]([CH2:6][C:7]2[CH:8]=[CH:9][C:10]3[C:19]4[NH:18][CH2:17][CH2:16][CH2:15][C:14]=4[C:13](=[O:20])[N:12](COC)[C:11]=3[CH:24]=2)=[N:4][N:3]=[N:2]1.[ClH:25]>C(O)C>[ClH:25].[NH:4]1[C:5]([CH2:6][C:7]2[CH:8]=[CH:9][C:10]3[C:19]4[NH:18][CH2:17][CH2:16][CH2:15][C:14]=4[C:13](=[O:20])[NH:12][C:11]=3[CH:24]=2)=[N:1][N:2]=[N:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 80 °C
Procedure
The compound (34 mg, 0.10 mmol) prepared in step 2 was dissolved in ethanol (5 ml), added with conc. hydrochloric acid (1.0 ml). The resulting mixture was stirred at 80° C. for 10 hours. Once the reaction was completed, the mixture concentrated under reduced pressure and filtered to obtain the title compound (28 mg, yield: 84%, yellow solid).
Workup
- concentrationthe mixture concentrated under reduced pressure
- filtrationfiltered
Sources & evidence
- ORD record
- ord-120bdae65dc74002bd0ede99dbf242c1
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08815891B2
Reaction notes
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