HCID 86656222, compound → HCID 67336520, compound
Reaction equation
C[O:2][C:3](=O)[CH:4]([C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[O:5][CH2:6][CH2:7][NH:8][NH:9]C(OC(C)(C)C)=O>O>[NH2:9][N:8]1[CH2:7][CH2:6][O:5][CH:4]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[C:3]1=[O:2]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
tert-Butyl 2-(2-(2-methoxy-2-oxo-1-phenylethoxy)ethyl)hydrazinecarboxylate (390 mg, 1.2 mmol) in water (85 mL) was heated to 95° C. for 12 h. The reaction mixture was extracted with dichloromethane, the organic layers were combined, dried over Na2SO4 and the solvent was evaporated to give the title compound as light yellow oil (183 mg, 79%).
Workup
- extractionThe reaction mixture was extracted with dichloromethane
- dry with materialdried over Na2SO4
- customthe solvent was evaporated
Sources & evidence
- ORD record
- ord-e3e877cfe7aa4337892b9df04da43635
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08486967B2
Reaction notes
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