Chloroform → HCID 57050471, compound

HRID 1462865Notes

Reaction equation

HRID 1462865 reaction equation
[CH2:1]([O:3][C:4]([C:6]1[C:11](=[O:12])[N:10]2[CH:13]([CH3:19])[CH2:14][CH2:15][C:16](=[N:17][NH2:18])[C:9]2=[N:8][CH:7]=1)=[O:5])[CH3:2].C(Cl)(Cl)Cl.C(N(CC)CC)C.[C:31](Cl)(=[O:38])[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1>O>[CH2:1]([O:3][C:4]([C:6]1[C:11](=[O:12])[N:10]2[CH:13]([CH3:19])[CH2:14][CH2:15][C:16](=[N:17][NH:18][C:31](=[O:38])[C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)[C:9]2=[N:8][CH:7]=1)=[O:5])[CH3:2]

Participants

6

Procedure

To a solution of 2.0 g. (7.57 millimoles) of ethyl-9-hydrazono-6-methyl-4-oxo-6,7,8,9-tetrahydro-4H-pyrido(1,2-a)pyrimidine-3-carboxylate and 20 ml. of anhydrous chloroform 1.6 ml. (11.35 millimoles) of triethylamine and 1.3 ml. (11.35 millimoles) of benzoyl chloride are added. The mixture is heated to boiling for 2 hours, whereupon it is cooled to room temperature and thoroughly admixed with 20 ml. of water. The organic phase is separated and the aqueous layer is extracted with 10 ml. of chloroform. The united organic phase is dried over anhydrous sodium sulfate and evaporated in vacuo. The residue is recrystallized from methanol. Thus 1.5 g. (53.8%) of ethyl-9-(benzoyl-hydrazono)-6-methyl-4-oxo-6,7,8,9-tetrahydro-4H-pyrido(1,2-a)pyrimidine-3-carboxylate are obtained. Mp.: 209°-210° C.

Workup

  1. temperatureThe mixture is heated
  2. customThe organic phase is separated
  3. extractionthe aqueous layer is extracted with 10 ml
  4. dry with materialThe united organic phase is dried over anhydrous sodium sulfate
  5. customevaporated in vacuo
  6. customThe residue is recrystallized from methanol

Sources & evidence

ORD record
ord-c72e3b5eecf748a18e66e41a548bb508
Source dataset
uspto-grants-1984_07
Patent number
US04461769

Reaction notes

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