HCID 10501216, compound → HCID 19607806, compound

HRID 745052Notes

Reaction equation

HRID 745052 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]>[Pd].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

5

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 liltrate 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 liltrate 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-600566f5c84f4dd89e673d2e3f6a093b
Source dataset
uspto-grants-1996_09
Patent number
US05559230

Reaction notes

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