BG63045B1 - Нови кумаринови производни,методи за получаванетоим и приложение - Google Patents
Нови кумаринови производни,методи за получаванетоим и приложение Download PDFInfo
- Publication number
- BG63045B1 BG63045B1 BG101722A BG10172297A BG63045B1 BG 63045 B1 BG63045 B1 BG 63045B1 BG 101722 A BG101722 A BG 101722A BG 10172297 A BG10172297 A BG 10172297A BG 63045 B1 BG63045 B1 BG 63045B1
- Authority
- BG
- Bulgaria
- Prior art keywords
- nhch
- general formula
- malonate
- amino
- coumarin derivative
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 10
- 238000002360 preparation method Methods 0.000 title claims abstract 3
- 150000001875 compounds Chemical class 0.000 claims abstract description 4
- -1 4-methyl-2-oxo-2H [1] -benzopyran-7-yl Chemical group 0.000 claims description 8
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 7
- 150000004775 coumarins Chemical class 0.000 claims description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
- LTMHNWPUDSTBKD-UHFFFAOYSA-N diethyl 2-(ethoxymethylidene)propanedioate Chemical compound CCOC=C(C(=O)OCC)C(=O)OCC LTMHNWPUDSTBKD-UHFFFAOYSA-N 0.000 claims description 4
- ONJZRBLUIQDRLI-UHFFFAOYSA-N chromen-2-one propanedioic acid Chemical class OC(=O)CC(O)=O.C1=CC=C2OC(=O)C=CC2=C1 ONJZRBLUIQDRLI-UHFFFAOYSA-N 0.000 claims description 2
- CFNMUZCFSDMZPQ-GHXNOFRVSA-N 7-[(z)-3-methyl-4-(4-methyl-5-oxo-2h-furan-2-yl)but-2-enoxy]chromen-2-one Chemical compound C=1C=C2C=CC(=O)OC2=CC=1OC/C=C(/C)CC1OC(=O)C(C)=C1 CFNMUZCFSDMZPQ-GHXNOFRVSA-N 0.000 claims 8
- 238000009835 boiling Methods 0.000 claims 1
- GLNDAGDHSLMOKX-UHFFFAOYSA-N coumarin 120 Chemical compound C1=C(N)C=CC2=C1OC(=O)C=C2C GLNDAGDHSLMOKX-UHFFFAOYSA-N 0.000 claims 1
- 230000004071 biological effect Effects 0.000 abstract description 2
- 230000015572 biosynthetic process Effects 0.000 abstract description 2
- 238000003786 synthesis reaction Methods 0.000 abstract description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- 238000004458 analytical method Methods 0.000 description 8
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N benzo-alpha-pyrone Natural products C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 6
- 238000005481 NMR spectroscopy Methods 0.000 description 5
- 230000035484 reaction time Effects 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- 235000001671 coumarin Nutrition 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- NFJDSQFWYOGGQU-UHFFFAOYSA-N 3-amino-8-fluorochromen-2-one Chemical compound C1=CC(F)=C2OC(=O)C(N)=CC2=C1 NFJDSQFWYOGGQU-UHFFFAOYSA-N 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- DHTLFPUVDPLEHP-UHFFFAOYSA-N CCC1=C(C(=O)OC2=C1C=C(C=C2)NC3OC(=O)CC(=O)O3)CC Chemical compound CCC1=C(C(=O)OC2=C1C=C(C=C2)NC3OC(=O)CC(=O)O3)CC DHTLFPUVDPLEHP-UHFFFAOYSA-N 0.000 description 2
- KFTYXCFUZNBMBT-UHFFFAOYSA-N CCC1=C(C=CC2=C1C(=C(C(=O)O2)O)CC)NC3OC(=O)CC(=O)O3 Chemical compound CCC1=C(C=CC2=C1C(=C(C(=O)O2)O)CC)NC3OC(=O)CC(=O)O3 KFTYXCFUZNBMBT-UHFFFAOYSA-N 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 229960000956 coumarin Drugs 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- BBVQKTUQIJKCAD-UHFFFAOYSA-N 3,4-diaminochromen-2-one Chemical compound C1=CC=CC2=C1OC(=O)C(N)=C2N BBVQKTUQIJKCAD-UHFFFAOYSA-N 0.000 description 1
- LALNOCKWGFCEEB-UHFFFAOYSA-N 6-amino-3-hydroxychromen-2-one Chemical compound O1C(=O)C(O)=CC2=CC(N)=CC=C21 LALNOCKWGFCEEB-UHFFFAOYSA-N 0.000 description 1
- ZOJAINJCZSVZGW-UHFFFAOYSA-N 6-aminochromen-2-one Chemical compound O1C(=O)C=CC2=CC(N)=CC=C21 ZOJAINJCZSVZGW-UHFFFAOYSA-N 0.000 description 1
- GXGJIOMUZAGVEH-UHFFFAOYSA-N Chamazulene Chemical group CCC1=CC=C(C)C2=CC=C(C)C2=C1 GXGJIOMUZAGVEH-UHFFFAOYSA-N 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 230000000259 anti-tumor effect Effects 0.000 description 1
- 230000000840 anti-viral effect Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/06—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2
- C07D311/08—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring
- C07D311/14—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring substituted in position 6 and unsubstituted in position 7
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/06—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2
- C07D311/08—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring
- C07D311/16—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring substituted in position 7
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/06—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2
- C07D311/08—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring
- C07D311/18—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring with oxygen or sulfur atoms directly attached in position 2 not hydrogenated in the hetero ring substituted otherwise than in position 3 or 7
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyrane Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HR960308A HRP960308A2 (en) | 1996-07-02 | 1996-07-02 | New coumarine derivatives, process for the preparation thereof and their use |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BG101722A BG101722A (en) | 1998-03-31 |
| BG63045B1 true BG63045B1 (bg) | 2001-02-28 |
Family
ID=10946423
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BG101722A BG63045B1 (bg) | 1996-07-02 | 1997-07-01 | Нови кумаринови производни,методи за получаванетоим и приложение |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US5840922A (cs) |
| EP (1) | EP0816353B1 (cs) |
| JP (1) | JPH1067768A (cs) |
| CN (1) | CN1170722A (cs) |
| AT (1) | ATE211136T1 (cs) |
| BA (1) | BA97239A (cs) |
| BG (1) | BG63045B1 (cs) |
| CA (1) | CA2209404A1 (cs) |
| CZ (1) | CZ207397A3 (cs) |
| DE (1) | DE69709252T2 (cs) |
| HR (1) | HRP960308A2 (cs) |
| HU (1) | HUP9701134A3 (cs) |
| PL (1) | PL320912A1 (cs) |
| PT (1) | PT816353E (cs) |
| RU (1) | RU2135490C1 (cs) |
| SI (1) | SI9700176B (cs) |
| SK (1) | SK282106B6 (cs) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1506359A (zh) * | 2002-12-05 | 2004-06-23 | �й�ҽѧ��ѧԺҩ���о��� | 新的香豆素酰胺衍生物及其制法和其药物组合物与用途 |
| CN1281599C (zh) * | 2003-05-15 | 2006-10-25 | 中国科学院上海有机化学研究所 | 香豆素类化合物和合成方法 |
| CN101747171A (zh) * | 2008-12-17 | 2010-06-23 | 上海药明康德新药开发有限公司 | 3-取代芳香基丙酸的快速合成方法 |
| CN101497593B (zh) * | 2009-03-18 | 2011-09-21 | 华南理工大学 | 5-羟基香豆素和吡喃型香豆素类化合物及合成方法与应用 |
| CN103420990B (zh) * | 2012-05-23 | 2016-04-20 | 复旦大学 | 7-氧、硫或氮杂取代香豆素及其衍生物和用途 |
| CN102898502B (zh) * | 2012-09-29 | 2014-07-23 | 首都医科大学 | 香豆素衍生物及其制备方法和应用 |
| CN104974122B (zh) * | 2015-07-02 | 2017-03-22 | 云南中烟工业有限责任公司 | 一种源自烟草的香豆素化合物、其制备方法和用途 |
| RU2733731C1 (ru) * | 2019-07-04 | 2020-10-06 | Федеральное государственное автономное образовательное учреждение высшего образования "Уральский федеральный университет имени первого Президента России Б.Н. Ельцина" | Способ получения промежуточных продуктов для синтеза каланолидов и их аналогов |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3313818A (en) * | 1965-04-14 | 1967-04-11 | Sterling Drug Inc | 7, 10-dihydro-3, 10-dioxo-7-(lower-alkyl)-3h-pyrano[3, 2-f]quinoline-3-carboxylic acid derivatives |
| NL7401012A (nl) * | 1974-01-25 | 1975-07-29 | Stamicarbon | Zuivering van cumarine en gealkyleerde derivaten hiervan. |
| US4210758A (en) * | 1979-03-21 | 1980-07-01 | Warner-Lambert Company | 1,5-Dihydro-1,5-dioxo-N-1H-tetrazol-5-yl-4H-[1]benzopyrano[3,4-b]pyridine-2-carboxamides |
| RU1623151C (ru) * | 1989-05-12 | 1996-01-10 | Научно-исследовательский институт фармакологии РАМН | Гидрохлориды производных 4-амино-3-[n-(аминоацетил)амино] кумарина, обладающие местно-анестезирующей активностью |
| EP0413152B1 (en) * | 1989-08-17 | 1996-01-10 | Abbott Laboratories | 7-Hydroxy coumarins having substitutions in the 4 position |
| HRP960352A2 (en) * | 1996-07-26 | 1998-08-31 | Pliva Pharm & Chem Works | Novel coumarin quinoline carboxylic acids |
-
1996
- 1996-07-02 HR HR960308A patent/HRP960308A2/hr not_active Application Discontinuation
-
1997
- 1997-06-27 BA BA970239A patent/BA97239A/bs unknown
- 1997-06-27 SK SK875-97A patent/SK282106B6/sk unknown
- 1997-06-28 CN CN97101199A patent/CN1170722A/zh active Pending
- 1997-06-30 CA CA002209404A patent/CA2209404A1/en not_active Abandoned
- 1997-06-30 CZ CZ972073A patent/CZ207397A3/cs unknown
- 1997-06-30 JP JP9174453A patent/JPH1067768A/ja active Pending
- 1997-07-01 RU RU97111207A patent/RU2135490C1/ru active
- 1997-07-01 AT AT97110824T patent/ATE211136T1/de not_active IP Right Cessation
- 1997-07-01 EP EP97110824A patent/EP0816353B1/en not_active Expired - Lifetime
- 1997-07-01 HU HU9701134A patent/HUP9701134A3/hu unknown
- 1997-07-01 BG BG101722A patent/BG63045B1/bg unknown
- 1997-07-01 PT PT97110824T patent/PT816353E/pt unknown
- 1997-07-01 DE DE69709252T patent/DE69709252T2/de not_active Expired - Fee Related
- 1997-07-02 PL PL97320912A patent/PL320912A1/xx unknown
- 1997-07-02 US US08/887,217 patent/US5840922A/en not_active Expired - Fee Related
- 1997-07-02 SI SI9700176A patent/SI9700176B/sl unknown
Also Published As
| Publication number | Publication date |
|---|---|
| HUP9701134A2 (hu) | 1998-12-28 |
| US5840922A (en) | 1998-11-24 |
| BA97239A (bs) | 2000-11-06 |
| CZ207397A3 (cs) | 1998-01-14 |
| DE69709252T2 (de) | 2002-07-25 |
| HRP960308A2 (en) | 1998-08-31 |
| HUP9701134A3 (en) | 2001-02-28 |
| HU9701134D0 (en) | 1997-08-28 |
| BG101722A (en) | 1998-03-31 |
| SK282106B6 (sk) | 2001-11-06 |
| EP0816353B1 (en) | 2001-12-19 |
| CA2209404A1 (en) | 1998-01-02 |
| SI9700176A (sl) | 1998-02-28 |
| PL320912A1 (en) | 1998-01-05 |
| PT816353E (pt) | 2002-05-31 |
| SI9700176B (sl) | 2002-02-28 |
| RU2135490C1 (ru) | 1999-08-27 |
| EP0816353A2 (en) | 1998-01-07 |
| CN1170722A (zh) | 1998-01-21 |
| SK87597A3 (en) | 1998-02-04 |
| JPH1067768A (ja) | 1998-03-10 |
| ATE211136T1 (de) | 2002-01-15 |
| EP0816353A3 (en) | 1998-03-04 |
| DE69709252D1 (de) | 2002-01-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4098788A (en) | Process for preparing quinazolines | |
| AU611997B2 (en) | 3,4 amino quinolines and 4 amino 3 nitroquinolines | |
| FI59991B (fi) | Foerfarande foer framstaellning av 2-arylamino-2-imidazolin-derivat och deras salter | |
| CZ20032654A3 (cs) | Způsob výroby 4,6-diaminopyrimido(5,4-d)pyrimidinů | |
| JPWO2003066602A1 (ja) | ４−アミノキナゾリン化合物の製法 | |
| BG63045B1 (bg) | Нови кумаринови производни,методи за получаванетоим и приложение | |
| HU195785B (en) | Process for production of 2-methil-4-amin-5-/formilamin-methil/-piramidine | |
| CA1243677A (en) | Process for the production of 4-amino-6,7-dimethoxy-2- [4-(furo-2-yl)-piperazin-1-yl]-quinazoline and physiologically compatible salts thereof | |
| FI86420C (fi) | Foerfarande foer framstaellning av 1-metylaminokinolin-karboxylsyraderivat. | |
| DK146625B (da) | 2-halogen-4-(beskyttet-amino)quinazolinderivater til anvendelse som mellemprodukter ved fremstilling af 2-(4-(2-furoyl)piperazin-1-yl)-4-amino-6,7-dimethoxyquinazolin | |
| Wright et al. | Analogs of pteroylglutamic acid. IV. Replacement of glutamic acid by other amino acids | |
| PT820998E (pt) | Novos acidos carboxilicos de benzopiranopiridona e processos para a sua preparacao | |
| El-Saghier | A novel one-pot synthesis of polyfunctionally substituted thiopyrano (2, 3-b) pyridine and pyrido (2, 3-b) pyridine derivatives under solid-liquid phase-transfer catalysis | |
| Zieliński et al. | A study concerning the synthesis, basicity and hydrolysis of 4‐amino‐2‐(N, N‐diethylamino) quinazoline derivatives | |
| Shemchuk et al. | Synthesis of N-(4-oxo-3, 4-dihydroquinazolin-3-yl) succinimide and N-(4-oxoquinazolin-3-yl) succinamic acid derivatives based thereon | |
| Patel et al. | Synthesis and biological evaluation of coumarinyl sydnone derivatives | |
| Spáčilová et al. | Synthesis of N‐amino‐3‐hydroxy‐2‐phenyl‐4 (1H)‐quinolinone | |
| US4568744A (en) | Benzylpyrimidine synthesis and intermediates | |
| US2428355A (en) | Amino-substituted acridines and method of making the same | |
| WO2008084493A2 (en) | A novel process for the preparation of 2-halo-4-aminoquinazolines | |
| JPS6241232B2 (cs) | ||
| JPH0651682B2 (ja) | ウラシル誘導体の製造方法 | |
| GB2161158A (en) | Benzylpyrimidine synthesis and intermediates | |
| NZ202320A (en) | Anthraniloyloxyalkanoates and pharmaceutical compositions containing such | |
| CS210394B1 (cs) | Deriváty formamidinu a způsoby jejich výroby |