Hydrochloric Acid → HCID 24798638, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][N:6]=[CH:5][C:4]=1[C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[N:14](COCC[Si](C)(C)C)[N:13]=[C:12]2[NH:26][C:27]1[N:31]([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[C:30]2[CH:38]=[CH:39][C:40]([CH2:42][OH:43])=[CH:41][C:29]=2[N:28]=1.Cl>C(O)C>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][N:6]=[CH:5][C:4]=1[C:9]1[CH:10]=[C:11]2[C:15](=[CH:16][CH:17]=1)[NH:14][N:13]=[C:12]2[NH:26][C:27]1[N:31]([C:32]2[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=2)[C:30]2[CH:38]=[CH:39][C:40]([CH2:42][OH:43])=[CH:41][C:29]=2[N:28]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
A mixture of (2-(5-(4-methoxypyridin-3-yl)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazol-3-ylamino)-1-phenyl-1H-benzo[d]imidazol-5-yl)methanol (0.024 g, 0.000040 mol) and 0.03 M HCl (1 mL,) in ethanol (3 mL) was heated at 100° C. for 2 hours. The reaction was concentrated and the residue was dissolved in DMSO and purified by HPLC.
Workup
- concentrationThe reaction was concentrated
- dissolutionthe residue was dissolved in DMSO
- custompurified by HPLC
Sources & evidence
- ORD record
- ord-d8650f12f42c4870bf6db31f75cfadbc
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08293923B2
Reaction notes
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