Reaction equation
[O:1]1[CH2:6][CH2:5][C:4](=O)[CH2:3][CH2:2]1.[C:8]([O:12][C:13](=[O:16])[NH:14][NH2:15])([CH3:11])([CH3:10])[CH3:9]>>[C:8]([O:12][C:13]([NH:14][N:15]=[C:4]1[CH2:5][CH2:6][O:1][CH2:2][CH2:3]1)=[O:16])([CH3:11])([CH3:10])[CH3:9]Participants
3
Procedure
B-22a was prepared analogously to B-19a starting from tetrahydro-4H-pyran-4-one (923 μL, 9.99 mmol) and tert-butylcarbazate (1.32 g, 9.99 mmol). Yield: 2.15 g.
Workup
- customB-22a was prepared analogously to B-19a
Sources & evidence
- ORD record
- ord-cf7565b56976401893de50b8aa10aee6
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08304556B2
Linked notes
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