Hydrochloric Acid → HCID 131737198, compound
Reaction equation
C(OC(=O)[NH:7][C:8]12[CH2:12][C:10]([C:13]([CH3:16])([CH3:15])[CH3:14])([CH2:11]1)[CH2:9]2)(C)(C)C.[ClH:18]>CCOC(C)=O>[Cl-:18].[C:13]([C:10]12[CH2:12][C:8]([NH2:7])([CH2:11]1)[CH2:9]2)([CH3:16])([CH3:15])[CH3:14]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of tert-butyl(3-(tert-butyl)bicyclo[1.1.1]pentan-1-yl)carbamate (0.983 g, 4.11 mmol) in EtOAc (10.3 mL) was treated with HCl (4.0M in dioxane, 41.1 mmol, 10.3 mL) and allowed to stir at r.t. overnight. The solution was concentrated under reduced pressure to afford the crude product as an off-white solid. The solid was triturated with Et2O (3×10 mL) to afford compound 15 as a white solid (0.6911 g). MS: m/z 140.2 [M+H]+.
Workup
- concentrationThe solution was concentrated under reduced pressure
- customto afford the crude product as an off-white solid
- customThe solid was triturated with Et2O (3×10 mL)
Sources & evidence
- ORD record
- ord-9492c261598242c9bb0dd7ecd54154e7
- Source dataset
- uspto-grants-2016_09
- Patent number
- US09447026B2
Reaction notes
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