Pyridine → Diethyl [(6-acetamido-4-quinazolinylamino)methylene]propanedioate

HRID 1719942Notes

Reaction equation

HRID 1719942 reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][N:6]=[C:5]2[NH:12][CH:13]=[C:14]([C:20]([O:22][CH2:23][CH3:24])=[O:21])[C:15]([O:17][CH2:18][CH3:19])=[O:16].N1C=CC=CC=1.[C:31](OC(=O)C)(=[O:33])[CH3:32]>ClCCl>[C:31]([NH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][N:6]=[C:5]2[NH:12][CH:13]=[C:14]([C:20]([O:22][CH2:23][CH3:24])=[O:21])[C:15]([O:17][CH2:18][CH3:19])=[O:16])(=[O:33])[CH3:32]

Participants

5

Reactant 3

HCID 1049PyridineHCID 7918Acetic AnhydrideHCID 20266113Diethyl[(6-amino-4-quinazolinylamino)methylene]propanedioate

Product 1

HCID 13060488Diethyl [(6-acetamido-4-quinazolinylamino)methylene]propanedioateYield 64.4%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

A mixture of diethyl [(6-amino-4-quinazolinylamino)methylene]propanedioate (3.03 g), pyridine (3.63 g) and dichloromethane (93 ml) was ice-cooled. To the mixture was added acetic anhydride (1.88 g). The reaction mixture was stirred for 30 minutes under ice-cooling and then for 2 hours and 15 minutes at ambient temperature. Ice water was added to the mixture. The resultant mixture was extracted with chloroform. The organic layer was washed three times with water and with aqueous solution saturated with sodium chloride, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give a residue, which was purified by a column chromatography on silica gel (developing solvent: chloroform) and recrystallized from chloroform, ethyl acetate and hexane to give crystalline diethyl [(6-acetamido-4-quinazolinylamino)methylene]propanedioate (2.2 g).

Workup

  1. temperaturecooled
  2. temperaturecooling
  3. waitfor 2 hours
  4. custom15 minutes
  5. customat ambient temperature
  6. extractionThe resultant mixture was extracted with chloroform
  7. washThe organic layer was washed three times with water
  8. dry with materialwith aqueous solution saturated with sodium chloride, dried over anhydrous magnesium sulfate
  9. concentrationconcentrated under reduced pressure
  10. customto give a residue, which
  11. customwas purified by a column chromatography on silica gel (developing solvent: chloroform)
  12. customrecrystallized from chloroform, ethyl acetate and hexane

Sources & evidence

ORD record
ord-42e1d32338864645b56ec5c30be81801
Source dataset
uspto-grants-1985_09
Patent number
US04543356

Reaction notes

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