HCID 10501216, compound → HCID 19607806, compound

HRID 1291613Notes

Reaction equation

HRID 1291613 reaction equation
[N+:1]([C:4]1[CH:5]=[C:6]([CH:28]=[CH:29][CH:30]=1)[C:7]([NH:9][C:10]1[CH:27]=[CH:26][C:13]([C:14]([N:16]2[C:25]3[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=3)[CH2:19][CH2:18][CH2:17]2)=[O:15])=[CH:12][CH:11]=1)=[O:8])([O-])=O.[H][H]>C(O)C>[NH2:1][C:4]1[CH:5]=[C:6]([CH:28]=[CH:29][CH:30]=1)[C:7]([NH:9][C:10]1[CH:27]=[CH:26][C:13]([C:14]([N:16]2[C:25]3[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=3)[CH2:19][CH2:18][CH2:17]2)=[O:15])=[CH:12][CH:11]=1)=[O:8]

Participants

4

Reactant 2

HCID 10501216HCID 10501216, compoundHCID 178418361HCID 178418361, compound

Product 1

HCID 19607806HCID 19607806, compoundYield 79.9%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

Ethanol (50 ml) is added to 10% Pd--C (0.1 g) and thereto is added-1-[4-(3-nitrobenzoylamino)benzoyl]-1,2,3,4-tetrahydroquinoline (0.73 g). The mixture is subjected to catalytic reduction at ordinary temperature under atmospheric pressure of hydrogen. After completion of the reduction, 10% Pd--C is removed by filtration and the filtrate is concentrated under reduced pressure. The residue is extracted with dichloromethane and the extract is dried over magnesium sulfate. The solvent is distilled off under reduced pressure and recrystallized from methanol to give 1-[4-(3-aminobenzoylamino)benzoyl]-1,2,3,4-tetrahydroquinoline (0.54 g) as white powder, m.p. 205.5°-206.5° C.

Workup

  1. customAfter completion of the reduction, 10% Pd--C is removed by filtration
  2. concentrationthe filtrate is concentrated under reduced pressure
  3. extractionThe residue is extracted with dichloromethane
  4. dry with materialthe extract is dried over magnesium sulfate
  5. distillationThe solvent is distilled off under reduced pressure
  6. customrecrystallized from methanol

Sources & evidence

ORD record
ord-298d5a8a480d42708f106122a7f7947d
Source dataset
uspto-grants-1998_05
Patent number
US05753677

Reaction notes

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