Hydrochloric Acid → HCID 71599697, compound
Reaction equation
Cl.C(OC([NH:9][C:10]1([C:40]([O:42][CH3:43])=[O:41])[CH2:15][CH2:14][N:13]([C:16]([C:18]2[CH:19]=[N:20][N:21]3[CH:26]=[CH:25][C:24]([N:27]4[CH2:31][CH2:30][CH2:29][C@@H:28]4[C:32]4[CH:37]=[C:36]([F:38])[CH:35]=[CH:34][C:33]=4[F:39])=[CH:23][C:22]=23)=[O:17])[CH2:12][CH2:11]1)=O)(C)(C)C>O1CCOCC1.O>[NH2:9][C:10]1([C:40]([O:42][CH3:43])=[O:41])[CH2:11][CH2:12][N:13]([C:16]([C:18]2[CH:19]=[N:20][N:21]3[CH:26]=[CH:25][C:24]([N:27]4[CH2:31][CH2:30][CH2:29][C@@H:28]4[C:32]4[CH:37]=[C:36]([F:38])[CH:35]=[CH:34][C:33]=4[F:39])=[CH:23][C:22]=23)=[O:17])[CH2:14][CH2:15]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 27.5 °C
Procedure
A mixture of 4M HCl solution in Dioxane (1 mL) and (R)-methyl 4-((tert-butoxycarbonyl)amino)-1-(5-(2-(2,5-difluorophenyl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyridine-3-carbonyl)piperidine-4-carboxylate (50 g, 0.085 mmol) was stirred at 20-35° C. for 3 h. After which the reaction mixture was concentrated under reduced pressure to afford the crude. The residue obtained was dissolved in water, extracted with ethylacetate, washed with saturated NaHCO3 solution followed by brine and dried over anhydrous sodium sulfate, concentrated under reduced pressure to afford 15 mg of the title compound.
Workup
- concentrationAfter which the reaction mixture was concentrated under reduced pressure
- customto afford the crude
- customThe residue obtained
- extractionextracted with ethylacetate
- washwashed with saturated NaHCO3 solution
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-2b6c01001a9e4b289334d7f5663ebc65
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09289419B2
Reaction notes
Loading…