SU1282510A1 - Substituted 1,2-dihydro-5-morpholino-4h-pyrano-[4′,3′:4,5]-pyrido-[2,3-b]-thieno-[3,2-d]-pyrimidine-8(9h)-one or -[9,11]-oxazine-8-one showing antibacterial effect - Google Patents
Substituted 1,2-dihydro-5-morpholino-4h-pyrano-[4′,3′:4,5]-pyrido-[2,3-b]-thieno-[3,2-d]-pyrimidine-8(9h)-one or -[9,11]-oxazine-8-one showing antibacterial effectInfo
- Publication number
- SU1282510A1 SU1282510A1 SU3914497/04;3922443/04A SU3914497A SU1282510A1 SU 1282510 A1 SU1282510 A1 SU 1282510A1 SU 3914497 A SU3914497 A SU 3914497A SU 1282510 A1 SU1282510 A1 SU 1282510A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- pyrano
- thieno
- morpholino
- dihydro
- pyrido
- Prior art date
Links
- 230000000844 anti-bacterial effect Effects 0.000 title 1
- 230000015572 biosynthetic process Effects 0.000 abstract 3
- 238000003786 synthesis reaction Methods 0.000 abstract 3
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 abstract 2
- 238000009835 boiling Methods 0.000 abstract 2
- 208000001848 dysentery Diseases 0.000 abstract 2
- 239000002244 precipitate Substances 0.000 abstract 2
- 241000193830 Bacillus <bacterium> Species 0.000 abstract 1
- 206010040047 Sepsis Diseases 0.000 abstract 1
- 241000191940 Staphylococcus Species 0.000 abstract 1
- 238000001816 cooling Methods 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 abstract 1
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- 208000013223 septicemia Diseases 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- JNMRHUJNCSQMMB-UHFFFAOYSA-N sulfathiazole Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=NC=CS1 JNMRHUJNCSQMMB-UHFFFAOYSA-N 0.000 abstract 1
- 229960001544 sulfathiazole Drugs 0.000 abstract 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
FIELD: fused heterocyclic compounds. SUBSTANCE: product: 1,2-dihydro-2,2-dimethyl-5-morpholino-4H-pyrano-[4′,3:4,5: 4,5] -pyrido-[2,3-b]-thieno-[3,2-d] -pyrimidine-8(9H)-one (I) or 1,2-dihydro-5-morpholino-8-oxo-2,2,10-trimethyl-4H-pyrano-[$$-$: 4,5]-pyrido-[2,3-b]-thieno-[3,2-d]-[9,11]-oxazine (II). Synthesis of (I) is carried out by boiling 3-amino-2-carbethoxy-5,5-dimethyl-8-(N-morpholino)-4,5-dihydro-7H-pyrano-[4,3-d]-thieno-[2,3-b]-pyridine and formamide for 2 h and precipitate is separated. The yield is 85.5% m. p. is 371-372 C, R0.68 (in dimethylformamide-ether, 2:5). Synthesis of (II) is carried out by boiling 3-amino-5,5-dimethyl-8-morpholino-2-carbethoxy-4,5-dihydro-7H- -pyrano-[4,3-d] -thieno-[2,3-b]-pyridine in the medium of (CHCO)O for 1 h. Precipitate is separated after cooling. The yield of (II) is 68.4% m. p. is 301-302 C. Effectiveness of (I) and (II) against staphylococcus and dysentery bacillus is at the level that of norsulfazole but at dysentery septicemia their effect is lower. EFFECT: improved method of synthesis. 1 tbl
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU3914497/04;3922443/04A SU1282510A1 (en) | 1985-06-18 | 1985-06-18 | Substituted 1,2-dihydro-5-morpholino-4h-pyrano-[4′,3′:4,5]-pyrido-[2,3-b]-thieno-[3,2-d]-pyrimidine-8(9h)-one or -[9,11]-oxazine-8-one showing antibacterial effect |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SU3914497/04;3922443/04A SU1282510A1 (en) | 1985-06-18 | 1985-06-18 | Substituted 1,2-dihydro-5-morpholino-4h-pyrano-[4′,3′:4,5]-pyrido-[2,3-b]-thieno-[3,2-d]-pyrimidine-8(9h)-one or -[9,11]-oxazine-8-one showing antibacterial effect |
Publications (1)
Publication Number | Publication Date |
---|---|
SU1282510A1 true SU1282510A1 (en) | 1995-09-20 |
Family
ID=60542789
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU3914497/04;3922443/04A SU1282510A1 (en) | 1985-06-18 | 1985-06-18 | Substituted 1,2-dihydro-5-morpholino-4h-pyrano-[4′,3′:4,5]-pyrido-[2,3-b]-thieno-[3,2-d]-pyrimidine-8(9h)-one or -[9,11]-oxazine-8-one showing antibacterial effect |
Country Status (1)
Country | Link |
---|---|
SU (1) | SU1282510A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2198888C2 (en) * | 1996-09-10 | 2003-02-20 | Басф Акциенгезелльшафт | 3-substituted derivatives of 3,4,5,6,7,8-hexahydro-pyrido-[4',3':4,5]-thieno[2,3- d]-pyrimidine |
RU2261251C2 (en) * | 2003-08-20 | 2005-09-27 | ООО "Исследовательский институт химического разнообразия" | Substituted 2h-pyrano[2,3-c]pyridines, combinatory and focused libraries |
EP1623987A1 (en) * | 2004-08-02 | 2006-02-08 | Curacyte Discovery GmbH | Fused pyrido[3',2':4,5]thieno[3,2-d]pyrimidines and pyrido[3',2':4,5]furo[3,2-d]pyrimidines |
-
1985
- 1985-06-18 SU SU3914497/04;3922443/04A patent/SU1282510A1/en active
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2198888C2 (en) * | 1996-09-10 | 2003-02-20 | Басф Акциенгезелльшафт | 3-substituted derivatives of 3,4,5,6,7,8-hexahydro-pyrido-[4',3':4,5]-thieno[2,3- d]-pyrimidine |
RU2261251C2 (en) * | 2003-08-20 | 2005-09-27 | ООО "Исследовательский институт химического разнообразия" | Substituted 2h-pyrano[2,3-c]pyridines, combinatory and focused libraries |
EP1623987A1 (en) * | 2004-08-02 | 2006-02-08 | Curacyte Discovery GmbH | Fused pyrido[3',2':4,5]thieno[3,2-d]pyrimidines and pyrido[3',2':4,5]furo[3,2-d]pyrimidines |
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