Ethanol hydrochloride → HCID 66976642, 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][OH:24])[CH:5]=[CH:6][C:7]=1[F:8].Cl.C(O)C>C(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][OH:24])[CH:5]=[CH:6][C:7]=1[F:8]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of tert-butyl (6RS,7SR)-7-(3-chloro-4-fluorophenyl)-6-(hydroxymethyl)-1,4-oxazepane-4-carboxylate (81 mg) in ethanol (1 mL) was added 14.7 N hydrogen chloride-ethanol solution (2.0 mL), and the mixture was stirred at room temperature for 1 hr. The crystals obtained by concentration under reduced pressure were recrystallized from ethyl acetate-ethanol to give the title compound (48 mg).
Workup
- customThe crystals obtained by concentration under reduced pressure
- customwere recrystallized from ethyl acetate-ethanol
Sources & evidence
- ORD record
- ord-7866f3b5894d4935b06cfb97815e45a8
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08722662B2
Reaction notes
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