Hydrogen chloride-ethyl acetate → HCID 66975207, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:9]2[O:15][CH2:14][CH2:13][N:12](C(OC(C)(C)C)=O)[CH2:11][CH:10]2[CH2:23][O:24][CH3:25])[CH:5]=[CH:6][C:7]=1[Cl:8].C(OCC)(=O)C.Cl>C(OCC)(=O)C>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([CH:9]2[O:15][CH2:14][CH2:13][NH:12][CH2:11][CH:10]2[CH2:23][O:24][CH3:25])[CH:5]=[CH:6][C:7]=1[Cl:8]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of tert-butyl (6RS,7RS)-7-(3,4-dichlorophenyl)-6-(methoxymethyl)-1,4-oxazepane-4-carboxylate (58 mg) in ethyl acetate (2 mL) was added 4 N hydrogen chloride-ethyl acetate solution (3.0 mL), and the mixture was stirred at room temperature for 2 hr. The crystals obtained by concentration under reduced pressure were recrystallized from ethanol to give the title compound (26.7 mg).
Workup
- customThe crystals obtained by concentration under reduced pressure
- customwere recrystallized from ethanol
Sources & evidence
- ORD record
- ord-afb2d385d80e484ba93de2cd3142c0db
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08722662B2
Reaction notes
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