Hydrochloric Acid → HCID 68008586, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:10]([C:11]3[N:16]=[C:15]([NH:17][C@H:18]4[CH2:23][CH2:22][CH2:21][C@@H:20]([NH:24][CH2:25][CH2:26][N:27](C)[C:28](=O)OC(C)(C)C)[CH2:19]4)[C:14]([F:36])=[CH:13][N:12]=3)=[CH:9][NH:8][C:5]2=[N:6][CH:7]=1.Cl.O1CCOCC1>ClCCl.CO>[Cl:1][C:2]1[CH:3]=[C:4]2[C:10]([C:11]3[N:16]=[C:15]([NH:17][C@H:18]4[CH2:23][CH2:22][CH2:21][C@@H:20]([NH:24][CH2:25][CH2:26][NH:27][CH3:28])[CH2:19]4)[C:14]([F:36])=[CH:13][N:12]=3)=[CH:9][NH:8][C:5]2=[N:6][CH:7]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
In a flask containing tert-butyl 2-((1R,3S)-3-(2-(5-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-5-fluoropyrimidin-4-ylamino)cyclohexylamino)ethyl(methyl)carbamate, 47b, (0.02 g, 0.04 mmol) in dichloromethane/MeOH mixture was added HCl in Dioxane (3.86 mL of 4 M solution, 15.44 mmol). The solution was stirred at room temperature for 12 hrs. The solvent was evaporated under reduced pressure and used without further purification.
Workup
- customThe solvent was evaporated under reduced pressure
- customused without further purification
Sources & evidence
- ORD record
- ord-bc2edfc35bf94d269045fc1b6d1882e8
- Source dataset
- uspto-grants-2016_05
- Patent number
- US09345708B2
Reaction notes
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