HCID 66658645, compound → HCID 54741065, compound
Reaction equation
C([O:5][C:6](=[O:27])[CH2:7][NH:8][C:9]([C:11]1[C:23](=[O:24])[N:22]([CH3:25])[C:14]2[N:15]=[N:16][C:17]([C:19]([OH:21])=[O:20])=[CH:18][C:13]=2[C:12]=1[OH:26])=[O:10])(C)(C)C.ClC1N=NC2N(C)C(=O)C(C(NCC(OC(C)(C)C)=O)=O)=C(O)C=2C=1>[Pd]>[C:6]([CH2:7][NH:8][C:9]([C:11]1[C:23](=[O:24])[N:22]([CH3:25])[C:14]2[N:15]=[N:16][C:17]([C:19]([OH:21])=[O:20])=[CH:18][C:13]=2[C:12]=1[OH:26])=[O:10])([OH:27])=[O:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
6-((2-tert-Butoxy-2-oxoethyl)carbamoyl)-5-hydroxy-8-methyl-7-oxo-7,8-dihydropyrido[2,3-c]pyridazine-3-carboxylic acid. The title compound is prepared by a palladium catalyzed carbonylation reaction of tert-butyl 2-(3-chloro-5-hydroxy-8-methyl-7-oxo-7,8-dihydropyrido[2,3-c]pyridazine-6-carboxamido)acetate according to the procedure of Tsuji, J., Palladium Reagents and catalysts: Innovations in Organic Synthesis Publisher: (Wiley, Chichester, UK), 340-45 (1995).
Sources & evidence
- ORD record
- ord-e45fbbdb912e49df9ee44684c7562b1d
- Source dataset
- uspto-grants-2012_01
- Patent number
- US08097620B2
Reaction notes
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