GB1328696A - 1-azazyclopentano-1,2-a-adamantane compounds and derivatives thereof - Google Patents
1-azazyclopentano-1,2-a-adamantane compounds and derivatives thereofInfo
- Publication number
- GB1328696A GB1328696A GB4133870A GB4133870A GB1328696A GB 1328696 A GB1328696 A GB 1328696A GB 4133870 A GB4133870 A GB 4133870A GB 4133870 A GB4133870 A GB 4133870A GB 1328696 A GB1328696 A GB 1328696A
- Authority
- GB
- United Kingdom
- Prior art keywords
- general formula
- adamantane
- alkyl
- group
- hydrogen atom
- 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
Links
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 6
- ORILYTVJVMAKLC-UHFFFAOYSA-N Adamantane Natural products C1C(C2)CC3CC1CC2C3 ORILYTVJVMAKLC-UHFFFAOYSA-N 0.000 abstract 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 abstract 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 3
- 238000010438 heat treatment Methods 0.000 abstract 3
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Substances ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 3
- KVBKBENCOHRLFW-UHFFFAOYSA-N 2-(2-adamantyl)acetic acid Chemical compound C1C(C2)CC3CC1C(CC(=O)O)C2C3 KVBKBENCOHRLFW-UHFFFAOYSA-N 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 abstract 2
- 235000019260 propionic acid Nutrition 0.000 abstract 2
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 abstract 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 2
- 235000011149 sulphuric acid Nutrition 0.000 abstract 2
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical compound C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 1
- 235000011054 acetic acid Nutrition 0.000 abstract 1
- 125000000218 acetic acid group Chemical class C(C)(=O)* 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- VLLNJDMHDJRNFK-UHFFFAOYSA-N adamantan-1-ol Chemical class C1C(C2)CC3CC2CC1(O)C3 VLLNJDMHDJRNFK-UHFFFAOYSA-N 0.000 abstract 1
- IYKFYARMMIESOX-UHFFFAOYSA-N adamantanone Chemical compound C1C(C2)CC3CC1C(=O)C2C3 IYKFYARMMIESOX-UHFFFAOYSA-N 0.000 abstract 1
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 abstract 1
- 230000001476 alcoholic effect Effects 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 230000003110 anti-inflammatory effect Effects 0.000 abstract 1
- 230000000840 anti-viral effect Effects 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 238000010531 catalytic reduction reaction Methods 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 238000005660 chlorination reaction Methods 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000003937 drug carrier Substances 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 229910052740 iodine Chemical group 0.000 abstract 1
- 150000003951 lactams Chemical class 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000012280 lithium aluminium hydride Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- -1 non-basic Substances 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- XUYJLQHKOGNDPB-UHFFFAOYSA-N phosphonoacetic acid Chemical compound OC(=O)CP(O)(O)=O XUYJLQHKOGNDPB-UHFFFAOYSA-N 0.000 abstract 1
- 238000006303 photolysis reaction Methods 0.000 abstract 1
- 230000015843 photosynthesis, light reaction Effects 0.000 abstract 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 abstract 1
- 238000006722 reduction reaction Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910001923 silver oxide Inorganic materials 0.000 abstract 1
- 239000012312 sodium hydride Substances 0.000 abstract 1
- 229910000104 sodium hydride Inorganic materials 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 abstract 1
- 239000001117 sulphuric acid Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/58—[b]- or [c]-condensed
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C53/00—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen
- C07C53/132—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen containing rings
- C07C53/136—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen containing rings containing condensed ring systems
- C07C53/138—Saturated compounds having only one carboxyl group bound to an acyclic carbon atom or hydrogen containing rings containing condensed ring systems containing an adamantane ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/26—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing rings other than six-membered aromatic rings
- C07C57/28—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing rings other than six-membered aromatic rings containing an adamantane ring system
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US85472469A | 1969-09-02 | 1969-09-02 | |
| US3490970A | 1970-05-04 | 1970-05-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1328696A true GB1328696A (en) | 1973-08-30 |
Family
ID=26711556
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4133870A Expired GB1328696A (en) | 1969-09-02 | 1970-08-27 | 1-azazyclopentano-1,2-a-adamantane compounds and derivatives thereof |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3624126A (https=) |
| JP (1) | JPS5017988B1 (https=) |
| CA (1) | CA974517A (https=) |
| CH (2) | CH532574A (https=) |
| DE (5) | DE2064905A1 (https=) |
| FR (1) | FR2070073B1 (https=) |
| GB (1) | GB1328696A (https=) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3879400A (en) * | 1973-11-16 | 1975-04-22 | Upjohn Co | 1-Lower alkyl-(1-adamantylmethyl)piperidines and process for their preparation |
| US3962328A (en) * | 1974-05-01 | 1976-06-08 | Kao Soap Co., Ltd. | Adamantyl thioamides |
| CA1248945A (en) * | 1983-03-15 | 1989-01-17 | George M. Kramer | Adamantyl carboxylic and sulfonic acid catalyzed paraffin-olefin alkylation and paraffin isomerization |
| US4745220A (en) * | 1986-05-27 | 1988-05-17 | Pennwalt Corporation | Substituted alpha-(2-tricyclo(3.3.1.13,7)-decylidene)benzeneacetamide derivatives |
| US4748264A (en) * | 1986-05-27 | 1988-05-31 | Pennwalt Corporation | Substituted alpha-[2'-tricyclo[3.3.1.13,7 ]-decylidene]benzeneacetonitrile derivatives |
| US4705891A (en) * | 1986-05-27 | 1987-11-10 | Pennwalt Corporation | Substituted α-[2'-tricyclo[3.3.1.13,7 ]decylidene]-benzeneacetic acid derivatives |
| GB2281274B (en) * | 1993-08-31 | 1997-04-09 | Johnson & Johnson Medical | Wound dressing package |
| AU2002322720B2 (en) | 2001-07-25 | 2008-11-13 | Raptor Pharmaceutical Inc. | Compositions and methods for modulating blood-brain barrier transport |
| CA2789262C (en) | 2005-04-28 | 2016-10-04 | Proteus Digital Health, Inc. | Pharma-informatics system |
| US7662831B2 (en) * | 2006-07-27 | 2010-02-16 | Wyeth Llc | Tetracyclic indoles as potassium channel modulators |
| US7601856B2 (en) * | 2006-07-27 | 2009-10-13 | Wyeth | Benzofurans as potassium ion channel modulators |
| EP2063905B1 (en) | 2006-09-18 | 2014-07-30 | Raptor Pharmaceutical Inc | Treatment of liver disorders by administration of receptor-associated protein (rap)-conjugates |
| TR201908314T4 (tr) | 2009-02-20 | 2019-06-21 | 2 Bbb Medicines B V | Glutatyon bazlı ilaç dağıtım sistemi. |
| KR101909711B1 (ko) | 2009-05-06 | 2018-12-19 | 라보라토리 스킨 케어, 인크. | 활성제-칼슘 포스페이트 입자 복합체를 포함하는 피부 전달 조성물 및 이들을 이용하는 방법 |
| US20120077778A1 (en) | 2010-09-29 | 2012-03-29 | Andrea Bourdelais | Ladder-Frame Polyether Conjugates |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3532748A (en) * | 1966-10-20 | 1970-10-06 | Du Pont | 2-adamantanamines |
| BE713610A (https=) * | 1968-04-12 | 1968-10-14 |
-
1970
- 1970-05-04 US US34909A patent/US3624126A/en not_active Expired - Lifetime
- 1970-08-25 CA CA091,488A patent/CA974517A/en not_active Expired
- 1970-08-27 GB GB4133870A patent/GB1328696A/en not_active Expired
- 1970-09-01 DE DE19702064905 patent/DE2064905A1/de active Pending
- 1970-09-01 DE DE19702064909 patent/DE2064909A1/de active Pending
- 1970-09-01 DE DE19702043380 patent/DE2043380A1/de active Pending
- 1970-09-01 DE DE19702064906 patent/DE2064906A1/de active Pending
- 1970-09-01 DE DE19702064904 patent/DE2064904A1/de active Pending
- 1970-09-02 CH CH1312870A patent/CH532574A/fr not_active IP Right Cessation
- 1970-09-02 JP JP45076987A patent/JPS5017988B1/ja active Pending
- 1970-09-02 CH CH1400371A patent/CH531476A/fr not_active IP Right Cessation
- 1970-09-02 FR FR7031950A patent/FR2070073B1/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| CA974517A (en) | 1975-09-16 |
| DE2064909A1 (de) | 1971-09-30 |
| US3624126A (en) | 1971-11-30 |
| DE2064906A1 (de) | 1972-01-20 |
| DE2064905A1 (https=) | 1972-01-13 |
| CH532574A (fr) | 1973-01-15 |
| DE2064904A1 (de) | 1971-11-25 |
| CH531476A (fr) | 1972-12-15 |
| FR2070073A1 (https=) | 1971-09-10 |
| JPS5017988B1 (https=) | 1975-06-25 |
| FR2070073B1 (https=) | 1977-01-28 |
| DE2043380A1 (de) | 1971-04-08 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB1328696A (en) | 1-azazyclopentano-1,2-a-adamantane compounds and derivatives thereof | |
| GB1180749A (en) | A New Polycyclic Amine and Processes for its Production | |
| ES246901A1 (es) | PROCEDIMIENTO PARA LA PREPARACION DE áCIDOS SULAMILANTRANiLICOS | |
| GB1254907A (en) | Indenyloxy and indenylthio alkanoic acids | |
| GB1291639A (en) | Xanthenyl alkanoic acid derivatives and pharmaceutical compositions containing them | |
| GB1307205A (en) | Isoindoline derivatives | |
| IE35424B1 (en) | Cyclopropane derivatives | |
| GB1325529A (en) | Aminophenylamidines their production and their medicinal use | |
| GB1273705A (en) | A method for producing 3,5-diaryl-4-pyrazole acetic acids | |
| IE34139L (en) | 4-phenyl-butyric acid derivatives | |
| GB1427114A (en) | Derivatives of 3- p-chlorobenoyl-2-methyl-phenylacetic acid | |
| GB1494988A (en) | Anti-inflammatory 1-oxoisoindoline derivatives and processes for their preparation | |
| GB1220599A (en) | New furazan derivatives, processes for their production and compositions containing them | |
| FR2103901A5 (https=) | ||
| GB1139164A (en) | New heterocyclic acetic acid compounds and methods for their production | |
| IE34016B1 (en) | New omikron-anilino-phenylethyl alcohols, the production thereof and compositions containing same | |
| GB1382438A (en) | Adamantane and substituted adamantane carboxylic acid esters of chloramphenicol | |
| GB1147832A (en) | Fluorene xanthene and thioxanthene derivatives | |
| GB1276719A (en) | Benzomorphan derivatives and their salts | |
| GB1440380A (en) | Pyrrolidine derivatives | |
| GB1391305A (en) | Phenylalkylamines | |
| GB1150397A (en) | New Indole-4-Acetic Acid Compounds and Methods for Their Production | |
| GB1271989A (en) | Adamantylideneacetanilide derivatives | |
| ES373529A1 (es) | Procedimiento para la preparacion de derivados de oxazolo (4,3-a) isoquinolina. | |
| GB1324500A (en) | Anti-inflammatory derivatives of 2- 3-trifluoromethyl-anilino- benzoic acid |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |