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

HRID 962543

反応式

HRID 962543 の反応式
[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]

参加物

5

反応物 3

HCID 313Hydrochloric AcidHCID 2199665,6-DihydrophenanthridineHCID 107074414-[(2-methylbenzoyl)amino]benzoyl Chloride

生成物 1

HCID 153079712-Methyl-N-[4-[(5(6H)-phenanthridinyl)carbonyl]phenyl]benzamide収率 18.9%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

実験手順

To a solution of 0.181 g (1.0 mmol) 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 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).

後処理

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

出典と根拠

ORDレコード
ord-68ef0fa7a5964731ad85617c54edad08
出典データセット
uspto-grants-1998_06
特許番号
US05760031

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