Hydrogen chloride-ethyl acetate → HCID 68578485, compound
Reaction equation
[CH3:1][S:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]1[C:19]2[O:18][CH2:17][CH2:16][N:15](C(OC(C)(C)C)=O)[CH2:14][C:13]=2[CH:12]=[CH:11][CH:10]=1.C(OCC)(=O)C.[ClH:33]>C(OCC)(=O)C>[ClH:33].[CH3:1][S:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]1[C:19]2[O:18][CH2:17][CH2:16][NH:15][CH2:14][C:13]=2[CH:12]=[CH:11][CH:10]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of tert-butyl 9-[2-(methylthio)phenyl]-2,3-dihydro-1,4-benzoxazepine-4(5H)-carboxylate (170 mg, 0.458 mmol), ethyl acetate (1 ml) and 4N hydrogen chloride-ethyl acetate solution (4 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 (133 mg, 94.3%) 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-a2831f38e7e849919f270cf399b07668
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08247403B2
Reaction notes
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