Hydrochloric Acid → HCID 58407625, compound
Reaction equation
[O:1]1CCCO[CH:2]1[C:7]1[CH:8]=[C:9]2[C:13](=[CH:14][CH:15]=1)[NH:12][N:11]=[C:10]2[N:16]([CH2:18][CH2:19][CH2:20][O:21][CH3:22])[CH3:17].Cl>C(O)C>[CH3:22][O:21][CH2:20][CH2:19][CH2:18][N:16]([CH3:17])[C:10]1[C:9]2[C:13](=[CH:14][CH:15]=[C:7]([CH:2]=[O:1])[CH:8]=2)[NH:12][N:11]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 90 °C
Procedure
To a solution of 131 mg (0.429 mmol) 5-(1,3-dioxan-2-yl)-N-(3-methoxypropyl)-N-methyl-1H-indazol-3-amine (Example 50A) in ethanol (7.0 ml) were added 1.43 ml (4.29 mmol) 3 M hydrochloric acid, and the solution was heated to 90° C. for 30 min. After cooling, the mixture was concentrated under reduced pressure. The remaining material (107 mg, 99% of th.) was used in the next step without further purification.
Workup
- temperatureAfter cooling
- concentrationthe mixture was concentrated under reduced pressure
- customThe remaining material (107 mg, 99% of th.) was used in the next step without further purification
Sources & evidence
- ORD record
- ord-ca262dcbdbc64cadb0aca88d21c5e5d9
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08551989B2
Reaction notes
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