HCID 54536067, compound → HCID 15410466, compound

HRID 1938210Notes

Reaction equation

HRID 1938210 reaction equation
[N+:1]([C:4]1[CH:25]=[CH:24][C:7]([C:8]([N:10]2[CH2:23][C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[C:16]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]2=3)=[O:9])=[CH:6][CH:5]=1)([O-])=O>C(OCC)(=O)C.[Pd]>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([C:8]([N:10]2[CH2:23][C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[C:16]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]2=3)=[O:9])=[CH:24][CH:25]=1

Participants

4

Reactant 1

HCID 54536067HCID 54536067, compound

Product 1

HCID 15410466HCID 15410466, compoundYield 87%

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 8857Ethyl AcetateSolvent

Procedure

A solution of 2.15 g of 5,6-dihydro-5-(4-nitrobenzoyl)phenanthridine in 50 ml of ethyl acetate and 0.5 g of 10% palladium-on-carbon is hydrogenated in a Parr apparatus under an atmosphere of hydrogen for three hours. The mixture is filtered through diatomaceous earth and the solvent removed to give 1.7 g of the product as a yellow foam.

Workup

  1. filtrationThe mixture is filtered through diatomaceous earth
  2. customthe solvent removed

Sources & evidence

ORD record
ord-39471094107c4adfb47147a19d786426
Source dataset
uspto-grants-1997_12
Patent number
US05693635

Reaction notes

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