ES8400432A1 - Preparation of pyridobenzoxazine derivative - Google Patents

Preparation of pyridobenzoxazine derivative

Info

Publication number
ES8400432A1
ES8400432A1 ES515608A ES515608A ES8400432A1 ES 8400432 A1 ES8400432 A1 ES 8400432A1 ES 515608 A ES515608 A ES 515608A ES 515608 A ES515608 A ES 515608A ES 8400432 A1 ES8400432 A1 ES 8400432A1
Authority
ES
Spain
Prior art keywords
compound
reaction
formula
solvent
prepared
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
ES515608A
Other languages
Spanish (es)
Other versions
ES515608A0 (en
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Daiichi Pharmaceutical Co Ltd
Original Assignee
Daiichi Pharmaceutical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Daiichi Pharmaceutical Co Ltd filed Critical Daiichi Pharmaceutical Co Ltd
Publication of ES515608A0 publication Critical patent/ES515608A0/en
Publication of ES8400432A1 publication Critical patent/ES8400432A1/en
Expired legal-status Critical Current

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  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

PURPOSE:To prepare the titled compound useful as an antibacterial agent, in high yield, purity and efficiency, e.g. by reacting a chelate compound of a pyridobenzoxazine derivative with a piperazine compound in one step. CONSTITUTION:The objective compound of formula III is prepared in one step by reacting the compound of formulaI(R1 is H or lower alkyl X1 and X2 are halogen) with a piperazine compound of formula II (R2 is H or lower alkyl). As an alternative method, it is prepared by decomposing the compound of formula IV obtained as an intermediate by the reaction of the above compounds. The reaction of the compound of formulaIwith the piperazine compound of formula II is carried out in the absence of solvent or in a solvent (e.g. acetone) and in the presence of an acid acceptor (e.g. TEA) usually at <=100 deg.C. When a ketone is used as the reaction solvent, and the reation is carried out at about its boiling point, or a the reaction is carried out in a polar aprotic solvent at <=room temperature for 0.5-5hr, then the compound of formula IV is obtained as the reaction product, and when the reaction is conducted in an aprotic polar solvent such as dimethylsulfoxide at 50-180 deg.C, the objective compound of formula III can be prepared in one step.
ES515608A 1981-09-09 1982-09-09 Preparation of pyridobenzoxazine derivative Expired ES8400432A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14191981A JPS5843977A (en) 1981-09-09 1981-09-09 Preparation of pyridobenzoxazine derivative

Publications (2)

Publication Number Publication Date
ES515608A0 ES515608A0 (en) 1983-11-01
ES8400432A1 true ES8400432A1 (en) 1983-11-01

Family

ID=15303207

Family Applications (1)

Application Number Title Priority Date Filing Date
ES515608A Expired ES8400432A1 (en) 1981-09-09 1982-09-09 Preparation of pyridobenzoxazine derivative

Country Status (9)

Country Link
JP (1) JPS5843977A (en)
AR (1) AR230451A1 (en)
DD (1) DD203719A5 (en)
DK (2) DK158268C (en)
ES (1) ES8400432A1 (en)
FI (1) FI76345C (en)
PL (1) PL130881B1 (en)
PT (1) PT75523B (en)
YU (2) YU43922B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1267413A (en) * 1984-04-26 1990-04-03 Abbott Laboratories Quino-benoxazine antibacterial compounds
CA1306750C (en) 1985-12-09 1992-08-25 Istvan Hermecz Process for the preparation of quinoline carboxylic acide
TW208013B (en) * 1990-03-01 1993-06-21 Daiichi Co Ltd

Also Published As

Publication number Publication date
JPS5843977A (en) 1983-03-14
FI823024L (en) 1983-03-10
DD203719A5 (en) 1983-11-02
YU74688A (en) 1989-12-31
FI76345B (en) 1988-06-30
YU202182A (en) 1984-12-31
AR230451A1 (en) 1984-04-30
PT75523B (en) 1984-12-12
FI76345C (en) 1988-10-10
DK173588D0 (en) 1988-03-29
PL238177A1 (en) 1983-05-09
YU43922B (en) 1989-12-31
YU46542B (en) 1993-11-16
FI823024A0 (en) 1982-09-01
ES515608A0 (en) 1983-11-01
PT75523A (en) 1982-10-01
DK158268B (en) 1990-04-23
JPH0148910B2 (en) 1989-10-20
DK158268C (en) 1990-10-15
DK399782A (en) 1983-03-10
PL130881B1 (en) 1984-09-29
DK173588A (en) 1988-03-29

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