Hydrochloric Acid → 2-Methyl-N-[4-[(5(6H)-phenanthridinyl)carbonyl]phenyl]benzamide

HRID 1957643Notes

Reaction equation

HRID 1957643 reaction equation
[CH:1]1[C:14]2[C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[CH2:7][NH:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.[CH3:15][C:16]1[CH:33]=[CH:32][CH:31]=[CH:30][C:17]=1[C:18]([NH:20][C:21]1[CH:29]=[CH:28][C:24]([C:25](Cl)=[O:26])=[CH:23][CH:22]=1)=[O:19].Cl>N1C=CC=CC=1>[CH3:15][C:16]1[CH:33]=[CH:32][CH:31]=[CH:30][C:17]=1[C:18]([NH:20][C:21]1[CH:29]=[CH:28][C:24]([C:25]([N:6]2[CH2:7][C:8]3[C:13](=[CH:12][CH:11]=[CH:10][CH:9]=3)[C:14]3[CH:1]=[CH:2][CH:3]=[CH:4][C:5]2=3)=[O:26])=[CH:23][CH:22]=1)=[O:19]

Participants

5

Procedure

To a solution of 0.181 g (1.0 immol) of 5,6-dihydrophenanthridine in 2 ml of warm pyridine is added 0.273 g (1.0 mmol) of 4-[(2-methylbenzoyl)amino]-benzoyl chloride. The mixture is stirred overnight at 30 room temperature, 1.2 ml of 2N HCl added. The solid which separates is filtered and washed with water. The solid is dissolved in dichloromethane and the solution washed with 2M sodium carbonate. The organic layer is concentrated and the residue chromatographed twice on silica gel with ethyl acetate-hexane as solvent to give 79 mg of crystals, m.p. 190°-194 ° C. Mass Spec-FAB 419 (M+H).

Workup

  1. additionadded
  2. filtrationThe solid which separates is filtered
  3. washwashed with water
  4. dissolutionThe solid is dissolved in dichloromethane
  5. washthe solution washed with 2M sodium carbonate
  6. concentrationThe organic layer is concentrated
  7. customthe residue chromatographed twice on silica gel with ethyl acetate-hexane as solvent

Sources & evidence

ORD record
ord-dee947bac9574bd7bf94141c371cb831
Source dataset
uspto-grants-1998_07
Patent number
US05786353

Reaction notes

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