Hydrogen chloride-ethyl acetate → HCID 68578362, compound
Reaction equation
[CH:1]([N:4]([CH3:23])[C:5]1[CH:22]=[CH:21][C:8]2[CH2:9][N:10](C(OC(C)(C)C)=O)[CH2:11][CH2:12][O:13][C:7]=2[CH:6]=1)([CH3:3])[CH3:2].C(OCC)(=O)C.[ClH:30]>>[ClH:30].[ClH:30].[CH:1]([N:4]([CH3:23])[C:5]1[CH:22]=[CH:21][C:8]2[CH2:9][NH:10][CH2:11][CH2:12][O:13][C:7]=2[CH:6]=1)([CH3:3])[CH3:2]Participants
3
Procedure
A solution of tert-butyl 8-[isopropyl(methyl)amino]-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate (270 mg, 0.843 mmol) in 4N hydrogen chloride-ethyl acetate (6 ml) was stirred for 1 hr at room temperature, and the solvent was evaporated under reduced pressure. The residue was recrystallized from a mixed solvent of methanol and ether to give the desired product (123 mg, 49.8%) as a solid.
Workup
- customthe solvent was evaporated under reduced pressure
- customThe residue was recrystallized from a mixed solvent of methanol and ether
Sources & evidence
- ORD record
- ord-27ad78b3bf1643c196d12ecd2067e406
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08247403B2
Reaction notes
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