HCID 10787818, compound → HCID 67753878, compound
Reaction equation
[OH:1][C@@H:2]1[C@@H:8]2[C@@H:5]([C:6](=[O:20])[N:7]2CC2C=CC(OC)=C(OC)C=2)[N:4]([C:21]([O:23][CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[O:22])[CH2:3]1.[Na].O=C1[C@@H]2[C@@H](CCN2C(OCC2C=CC=CC=2)=O)N1S(O)(=O)=O>>[OH:1][C@@H:2]1[C@@H:8]2[C@@H:5]([C:6](=[O:20])[NH:7]2)[N:4]([C:21]([O:23][CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[O:22])[CH2:3]1Participants
3
Procedure
Benzyl (1S,4S,5S)-4-hydroxy-7-oxo-2,6-diazabicyclo-[3.2.0]heptane-2-carboxylate was prepared from benzyl (1S,4S,5S)-4-hydroxy -6-(3,4-dimethoxybenzyl)-7-oxo-2,6-diazabicyclo-[3.2.0]heptane-2-carboxylate (Example 1) in the same manner as described for benzyl (1S,5R)-7-oxo-2,6-diazabicyclo[3.2.0]heptane-2-carboxylate (Example 1).
Sources & evidence
- ORD record
- ord-027205f1c8ba445f8f266949f3818120
- Source dataset
- uspto-grants-1998_01
- Patent number
- US05712268
Reaction notes
Loading…