Sodium Acetate → HCID 22632742, compound
Reaction equation
Cl.[Cl:2][C:3]1[CH:8]=[C:7]([C:9]2[O:10][CH2:11][C:12](=[O:21])[N:13]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[N:14]=2)[CH:6]=[CH:5][N:4]=1.C([O-])(=O)C.[Na+]>CO.[Pd]>[ClH:2].[N:4]1[CH:5]=[CH:6][C:7]([C:9]2[O:10][CH2:11][C:12](=[O:21])[N:13]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[N:14]=2)=[CH:8][CH:3]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
2-(2-Chloro-4-pyridyl)-4-phenyl-4H-1,3,4-oxadiazine-5(6H)-one hydrochloride (780 mg, 2.4 mmol) obtained in Example 12 was hydrogenated in a usual manner in methanol in the presence of sodium acetate and 10% palladium/carbon catalyst, to give the title compound (230 mg, yield 33%).
Sources & evidence
- ORD record
- ord-94d7cc01c10341d0927b3bd4f2a59b8c
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06825192B1
Reaction notes
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