6,7-Dihydro-5H-1-pyridin-5-one → (5Z)-N-Hydroxy-6,7-dihydro-5H-cyclopenta[b]pyridin-5-imine
Reaction equation
O1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)/[C:4](=[N:11]/[OH:12])/[CH2:3]C1.[N:13]1C=CC=C2C(=O)CCC=12>>[N:13]1[CH:8]=[CH:7][CH:6]=[C:5]2/[C:4](=[N:11]\[OH:12])/[CH2:3][CH2:9][C:10]=12Participants
3
Procedure
Following the procedure for the preparation of (4E)-2,3-dihydro-4H-chromen-4-one oxime but substituting 6,7-dihydro-5H-cyclopenta[b]pyridin-5-one and making non-critical variations provided the title compound as a oil: 1H NMR (400 MHz, DMSO-d6) δ) 11.11, 8.50, 7.89, 7.27, 3.04, 2.81; HRMS (EI) calcd for C8H8N2O 148.0637, found 148.0628.
Sources & evidence
- ORD record
- ord-5a92c95669d54213ae0ea79459ab03aa
- Source dataset
- uspto-grants-2006_01
- Patent number
- US06992087B2
Reaction notes
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