KR830005219A - 페닐-퀴놀리지딘 - Google Patents
페닐-퀴놀리지딘 Download PDFInfo
- Publication number
- KR830005219A KR830005219A KR1019810001230A KR810001230A KR830005219A KR 830005219 A KR830005219 A KR 830005219A KR 1019810001230 A KR1019810001230 A KR 1019810001230A KR 810001230 A KR810001230 A KR 810001230A KR 830005219 A KR830005219 A KR 830005219A
- Authority
- KR
- South Korea
- Prior art keywords
- formula
- compound
- hydrogen
- structural formula
- following structural
- 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.)
- Withdrawn
Links
- OUZYKKYJPBLWGM-UHFFFAOYSA-N 1-phenyl-2,3,4,6,7,8,9,9a-octahydro-1h-quinolizine Chemical compound C12CCCCN2CCCC1C1=CC=CC=C1 OUZYKKYJPBLWGM-UHFFFAOYSA-N 0.000 title claims 2
- 150000001875 compounds Chemical class 0.000 claims 7
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- 239000001257 hydrogen Substances 0.000 claims 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- -1 acetate ester Chemical class 0.000 claims 3
- 125000002252 acyl group Chemical group 0.000 claims 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 239000001301 oxygen Substances 0.000 claims 3
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 2
- 238000007126 N-alkylation reaction Methods 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 125000004442 acylamino group Chemical group 0.000 claims 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
- 229910052794 bromium Inorganic materials 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 239000000460 chlorine Chemical group 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 239000011737 fluorine Chemical group 0.000 claims 2
- 150000002431 hydrogen Chemical group 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 claims 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims 1
- 101001053395 Arabidopsis thaliana Acid beta-fructofuranosidase 4, vacuolar Proteins 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- QGJOPFRUJISHPQ-NJFSPNSNSA-N carbon disulfide-14c Chemical compound S=[14C]=S QGJOPFRUJISHPQ-NJFSPNSNSA-N 0.000 claims 1
- 150000003857 carboxamides Chemical class 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- 238000009833 condensation Methods 0.000 claims 1
- RAFNCPHFRHZCPS-UHFFFAOYSA-N di(imidazol-1-yl)methanethione Chemical compound C1=CN=CN1C(=S)N1C=CN=C1 RAFNCPHFRHZCPS-UHFFFAOYSA-N 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 238000005984 hydrogenation reaction Methods 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 239000011630 iodine Substances 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 230000003647 oxidation Effects 0.000 claims 1
- 238000007254 oxidation reaction Methods 0.000 claims 1
- 125000004043 oxo group Chemical group O=* 0.000 claims 1
- CYQAYERJWZKYML-UHFFFAOYSA-N phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 claims 1
- 150000003141 primary amines Chemical class 0.000 claims 1
- 238000006798 ring closing metathesis reaction Methods 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D455/00—Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH2784/80 | 1980-04-11 | ||
| CH278480 | 1980-04-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR830005219A true KR830005219A (ko) | 1983-08-03 |
Family
ID=4241517
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019810001230A Withdrawn KR830005219A (ko) | 1980-04-11 | 1981-04-10 | 페닐-퀴놀리지딘 |
Country Status (7)
| Country | Link |
|---|---|
| JP (1) | JPS56158783A (enExample) |
| KR (1) | KR830005219A (enExample) |
| BR (1) | BR8102218A (enExample) |
| CS (1) | CS222700B2 (enExample) |
| ES (4) | ES512072A0 (enExample) |
| GR (1) | GR74868B (enExample) |
| ZA (1) | ZA812285B (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3737680A1 (en) * | 2018-01-08 | 2020-11-18 | F. Hoffmann-La Roche AG | Octahydropyrido[1,2-alpha]pyrazines as magl inhibitors |
-
1981
- 1981-04-03 ZA ZA00812285A patent/ZA812285B/xx unknown
- 1981-04-08 JP JP5189681A patent/JPS56158783A/ja active Pending
- 1981-04-09 GR GR64631A patent/GR74868B/el unknown
- 1981-04-10 BR BR8102218A patent/BR8102218A/pt unknown
- 1981-04-10 KR KR1019810001230A patent/KR830005219A/ko not_active Withdrawn
- 1981-04-13 CS CS818809A patent/CS222700B2/cs unknown
-
1982
- 1982-05-11 ES ES512072A patent/ES512072A0/es active Granted
- 1982-05-11 ES ES512074A patent/ES512074A0/es active Granted
- 1982-05-11 ES ES512073A patent/ES512073A0/es active Granted
- 1982-05-11 ES ES512071A patent/ES8302703A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| ES8302707A1 (es) | 1983-02-01 |
| ES512071A0 (es) | 1983-02-01 |
| ES8302704A1 (es) | 1983-02-01 |
| ES8302706A1 (es) | 1983-02-01 |
| ES512074A0 (es) | 1983-02-01 |
| GR74868B (enExample) | 1984-07-12 |
| ES8302703A1 (es) | 1983-02-01 |
| CS222700B2 (en) | 1983-07-29 |
| JPS56158783A (en) | 1981-12-07 |
| ZA812285B (en) | 1982-04-28 |
| ES512073A0 (es) | 1983-02-01 |
| ES512072A0 (es) | 1983-02-01 |
| BR8102218A (pt) | 1981-10-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR840004406A (ko) | 히단토인의 제조방법 | |
| KR870003998A (ko) | 퀴나졸린 유도체류의 제조방법 | |
| DE3773089D1 (de) | Verfahren zur herstellung von thiazolidinedion-derivaten. | |
| KR830006228A (ko) | 이미다졸 유도체의 제조방법 | |
| KR830005148A (ko) | 항 알러지성 이미도디설파마이드의 제조방법 | |
| DE3576955D1 (de) | Beta-carbolin-3-oxadiazolylderivate, verfahren zu ihrer herstellung und ihre verwendung. | |
| KR840000463A (ko) | 광학적으로 활성인 1-방향족 그룹으로 치환된-1- 알카논의 제조방법 | |
| KR830006906A (ko) | 시클로로프로판 카르복실레이트의 제조방법 | |
| KR830002722A (ko) | 이미다졸리딘 유도체의 제조방법 | |
| ATE10838T1 (de) | 4-substituierte 2-oxoazetidin-verbindungen, verfahren zu deren herstellung und ihre verwendung zur antibiotika-herstellung. | |
| ATE53583T1 (de) | Beta-carbolin-3-carbonsaeurederivate, verfahren zu ihrer herstellung und ihre verwendung. | |
| KR860003240A (ko) | 1,2,4- 트리아졸로- 카바메이트의 제조방법 | |
| ATE31414T1 (de) | 8-substituierte pyrrolizidin-derivate und deren verwendung. | |
| KR830005219A (ko) | 페닐-퀴놀리지딘 | |
| PT86258A (de) | Imidazolderivate und ein verfahren zu deren herstellung | |
| KR840001577A (ko) | 복소환식 화합물의 제조방법 | |
| KR870007127A (ko) | 퀴놀론 카복실산 유도체의 제조방법 | |
| KR830005218A (ko) | 2-[3-[4-(3-클로로-4-플루오로페닐)-1-피페라지닐]프로필]-1,2,4-트리아졸로[4,3-a]피리딘-3(2H)-온 | |
| KR830006302A (ko) | 신규 피리미딘 유도체의 제조방법 | |
| KR840001974A (ko) | 1-[3-(6-플루오로-1,2-벤즈이속사졸-3-일)프로필]-4-(치환된)-피페라진 및-피레리딘의 제조방법 | |
| KR860002486A (ko) | 티아진포스폰산 유도체의 제조방법 | |
| ES481264A1 (es) | Procedimiento para fabricar derivados del acido arilacetico. | |
| KR840000551A (ko) | 이미다조[1, 2-a]피리미딘의 제조방법 | |
| KR890002011A (ko) | 5-할로 게노-6-아미노-니코틴산 할라이드. 이의 제조방법 및 용도 | |
| KR830005225A (ko) | 데오필린의 피페라진 유도체의 제조방법 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 19810410 |
|
| PG1501 | Laying open of application | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 19840426 Patent event code: PE09021S01D |
|
| PC1203 | Withdrawal of no request for examination |