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ChemicalBook >  Product Catalog >  Organic Chemistry >  Carboxylic acids and derivatives >  Ethyl 6-fluoro-1-methyl-4-oxo-7-(1-piprazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate

Ethyl 6-fluoro-1-methyl-4-oxo-7-(1-piprazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate

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Ethyl 6-fluoro-1-methyl-4-oxo-7-(1-piprazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate Basic information

Product Name:
Ethyl 6-fluoro-1-methyl-4-oxo-7-(1-piprazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate
Synonyms:
  • 6-FLUORO-1-METHYL-4-OXO-7-(1-PIPERAZINYL)-4H-(1,3)THIAZETO(3,2-A)QUINOLINE-3-CARBOYLIC ACID ETHYL ESTER
  • 6-FLUORO-1-METHYL-4-OXO-7-(1-PIPRAZINYL)-1H,4H-(1,3)THIAZETO(3,2-A)QUINOLINE-3-CARBOXYLIC ACID, ETHYL ESTER
  • ethyl 6-fluoro-1-methyl-4-oxo-7-(piperazin-1-yl)-1H,4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate
  • 6-Fluoro-1-methyl-4-oxo-7-(1-piperazinyl)-1H,4H-[1,3]-thiazeto[3,2-a]-3-quinolinecarboxylic acid ethyl ester
  • Ethyl 6-fluoro-1-methyl-4-oxo-7-(1-piprazinyl)-4H-(1,3)-thiazeto(3,2-a)
  • ETHYL 6-FLUORO-1-METHYL-4-OXO-7-(1-PIPERAZINYL)-4H-(1,3)-THIAZETO(3,2-A) QUINOLINE-3-CARBOXYLATE
  • Prulifloxacin Intermediate PL-10
  • Ethyl 6-fluoro-1-Methyl-4-oxo-7-(piperazin-1-yl)-1,4-dihydro-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate
CAS:
113028-17-4
MF:
C18H20FN3O3S
MW:
377.43
EINECS:
601-222-6
Product Categories:
  • Other Products
  • API intermediates
  • PRULIFLOXACIN
Mol File:
113028-17-4.mol
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Ethyl 6-fluoro-1-methyl-4-oxo-7-(1-piprazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate Chemical Properties

Melting point:
224 °C
Boiling point:
579.1±50.0 °C(Predicted)
Density 
1.44±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
8.69±0.10(Predicted)
CAS DataBase Reference
113028-17-4(CAS DataBase Reference)
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Ethyl 6-fluoro-1-methyl-4-oxo-7-(1-piprazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate Usage And Synthesis

Uses

Ethyl 6-fluoro-1-methyl-4-oxo-7-(1-piprazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate is an off-white to slightly yellow powder used as an intermediate for prulifloxacin.

Synthesis

110-85-0

113046-72-3

113028-17-4

The general procedure for the synthesis of ethyl 6-fluoro-7-piperazine-1-methyl-4-oxo-1,4-dihydro-[1,3]thiazepine[3,2-a]quinoline-3-carboxylate from ethyl 6,7-difluoro-1-methyl-4-oxo-1,4-dihydro-[1,3]thiazepine[3,2-a]quinoline-3-carboxylate and piperazine was carried out as follows: 50 g of ethyl 6,7-difluoro-1-methyl-4 -oxo-4H-[1,3]thiazino[3,2-a]quinoline-3-carboxylic acid ethyl ester was dissolved in 5 volumes of DMSO and heated to 60 °C. Subsequently, 40 g of piperazine was added and the reaction was kept stirred at 60°C for 4 hours. After completion of the reaction, the mixture was cooled to room temperature, 5 volumes of acetonitrile was added and stirring was continued at room temperature for 4 hours. The precipitate was collected by filtration and dried to give 52.8 g of ethyl 6-fluoro-7-piperazine-1-methyl-4-oxo-[1,3]thiazolocyclo[3,2-a]quinoline-3-carboxylate in 87% yield. After further purification, the yield of ethyl 6-fluoro-7-piperazine-1-methyl-4-oxo-[1,3]thiazolocyclo[3,2-a]quinoline-3-carboxylate was up to 99%.

References

[1] Patent: CN107383069, 2017, A. Location in patent: Paragraph 0061; 0062
[2] Patent: CN107501298, 2017, A. Location in patent: Paragraph 0055; 0056
[3] Journal of Medicinal Chemistry, 1992, vol. 35, # 25, p. 4727 - 4738
[4] Patent: US4843070, 1989, A
[5] Patent: WO2009/93268, 2009, A1. Location in patent: Page/Page column 15

Ethyl 6-fluoro-1-methyl-4-oxo-7-(1-piprazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylateSupplier

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