HCID 86750594, compound → HCID 19964384, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[C:15](/[CH:16]=[CH:17]/[C:18]([O:20][CH3:21])=[O:19])=[C:14]3[N:9]([CH2:10][CH2:11][C:12]4[CH:25]=[CH:24][CH:23]=[CH:22][C:13]=43)[C:8](=[O:26])[C:7]=2[CH:27]=1>C(O)(=O)C.[Pd]>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[C:15]([CH2:16][CH2:17][C:18]([O:20][CH3:21])=[O:19])=[C:14]3[N:9]([CH2:10][CH2:11][C:12]4[CH:25]=[CH:24][CH:23]=[CH:22][C:13]=43)[C:8](=[O:26])[C:7]=2[CH:27]=1Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 3.5 g (9.68 mmol) of methyl (E)-3-(10-methoxy-8-oxo-5,8-dihydro-6H-dibenzo[a,g]quinolizin-13-yl)prop-2-enoate in 100 ml of acetic acid is added 0.5 g of 5% palladium on charcoal and the suspension is subjected to hydrogenation in a Parr apparatus at a pressure of about 0.32 MPa between 50° and 60° C. for 3 h.
Sources & evidence
- ORD record
- ord-04fcf7b84c164d10ad93d80410566938
- Source dataset
- uspto-grants-1997_03
- Patent number
- US05614517
Reaction notes
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