Morpholine → HCID 13044301, compound

HRID 1583616Notes

Reaction equation

HRID 1583616 reaction equation
[F:1][C:2]1[CH:14]=[C:12]2[C:13]3[N:8]([CH:9]=[C:10]([C:16]([OH:18])=[O:17])[C:11]2=[O:15])[CH:7]([CH3:19])[CH2:6][CH2:5][C:4]=3[C:3]=1Br.[NH:21]1[CH2:26][CH2:25][O:24][CH2:23][CH2:22]1.CN(C)P(=O)(N(C)C)N(C)C>C(OCC)(=O)C>[F:1][C:2]1[CH:14]=[C:12]2[C:13]3[N:8]([CH:9]=[C:10]([C:16]([OH:18])=[O:17])[C:11]2=[O:15])[CH:7]([CH3:19])[CH2:6][CH2:5][C:4]=3[C:3]=1[N:21]1[CH2:26][CH2:25][O:24][CH2:23][CH2:22]1

Participants

5

Procedure

In a 200 ml stainless steel autoclave were placed 10 g of 9-fluoro-8-bromo-5-methyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid, 12.8 g of morpholine and 80 ml of hexamethylphosphoric triamide and the mixture was reacted at 160° C. on an oil bath. After 7 hours, the temperature of the autoclave was lowered to room temperature and disappearance of the starting materials was confirmed by thin layer chromatography. Then, the reaction mixture was transferred from the autoclave to a 300 ml Erlenmeyer flask to which ethyl acetate was added and the resulting mixture was allowed to stand for 1 day. The crystals which formed were collected by filtration and recrystallized from dimethylformamide to give 4 g of 9-fluoro-8-morpholino-5-methyl-6,7-dihydro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid. m.p. 279°-280° C., white rhombic crystals.

Workup

  1. customthe mixture was reacted at 160° C. on an oil bath
  2. customwas lowered to room temperature
  3. additionwas added
  4. waitto stand for 1 day
  5. customThe crystals which formed
  6. filtrationwere collected by filtration
  7. customrecrystallized from dimethylformamide

Sources & evidence

ORD record
ord-1d7d163f24a4483ba25b969a9bfd74de
Source dataset
uspto-grants-1985_11
Patent number
US04552879

Reaction notes

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