HCID 89851371, compound → (2S,5R)-6-(allyloxy)-4-cyclopropyl-7-oxo-1,6-diazabicyclo[3.2.1]oct-3-ene-2-carboxamide
Reaction equation
[CH2:1]([O:4][NH:5][CH:6]1[CH2:11][NH:10][C@@H:9]([C:12]([NH2:14])=[O:13])[CH:8]=[C:7]1[CH:15]1[CH2:17][CH2:16]1)[CH:2]=[CH2:3].[CH2:18]([O:21]N1C(=O)N2C[C@H]1C(C)=C[C@H]2C(N)=O)C=C>>[CH2:1]([O:4][N:5]1[C:18](=[O:21])[N:10]2[CH2:11][C@H:6]1[C:7]([CH:15]1[CH2:16][CH2:17]1)=[CH:8][C@H:9]2[C:12]([NH2:14])=[O:13])[CH:2]=[CH2:3]Participants
3
Procedure
The title compound was prepared from (R)-5-(allyloxyamino)-4-cyclopropyl-1,2,5,6-tetrahydropyridine-2-carboxamide (Intermediate 270, 0.307 g, 1.29 mmol) following the procedure described for Intermediate 16. The desired product was obtained as a yellow oil (0.168 g, 49%).
Sources & evidence
- ORD record
- ord-8e372b0dfc884aceb33c49c219f99a38
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09309245B2
Reaction notes
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