HCID 15858811, compound → HCID 21309376, compound
Reaction equation
C(OC([NH:11][C@@H:12]1[C:18](=[O:19])[N:17]2[C@@H:13]1[O:14][CH2:15][CH2:16]2)=O)C1C=CC=CC=1.[H][H]>[Pd].C(OCC)(=O)C>[NH2:11][C@@H:12]1[C:18](=[O:19])[N:17]2[C@@H:13]1[O:14][CH2:15][CH2:16]2Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
(5R,6S)-6-benzyloxycarbonylamino-4-oxa-1-azabicyclo[3,2,0]heptan-7-one (950 mg, 3.624 mmole) was hydrogenated with 3 g of 10% palladium on activated carbon in ethyl acetate (80 ml) at 50 psi hydrogen pressure at room temperature for 6 hrs. after removal of catalyst by filtration, deprotected (5R,6S)-6-amino-4-oxa-1-azabicyclo[3,2,0]heptan-7-one in ethyl acetate was obtained.
Workup
- customafter removal of catalyst
- filtrationby filtration
Sources & evidence
- ORD record
- ord-0d6a757672814a92819b2ee952758d81
- Source dataset
- uspto-grants-1999_05
- Patent number
- US05905076
Reaction notes
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