GB1332930A - Acyl derivatives of substituted bis-arylalklamines - Google Patents
Acyl derivatives of substituted bis-arylalklaminesInfo
- Publication number
- GB1332930A GB1332930A GB6019370A GB6019370A GB1332930A GB 1332930 A GB1332930 A GB 1332930A GB 6019370 A GB6019370 A GB 6019370A GB 6019370 A GB6019370 A GB 6019370A GB 1332930 A GB1332930 A GB 1332930A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- compounds
- alkyl
- reacting
- methylphenethylamino
- 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
- 125000002252 acyl group Chemical group 0.000 title abstract 5
- 150000001875 compounds Chemical class 0.000 abstract 8
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 125000004423 acyloxy group Chemical group 0.000 abstract 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- ARKIFHPFTHVKDT-UHFFFAOYSA-N 1-(3-nitrophenyl)ethanone Chemical compound CC(=O)C1=CC=CC([N+]([O-])=O)=C1 ARKIFHPFTHVKDT-UHFFFAOYSA-N 0.000 abstract 1
- KUIZKZHDMPERHR-UHFFFAOYSA-N 1-phenylprop-2-en-1-one Chemical compound C=CC(=O)C1=CC=CC=C1 KUIZKZHDMPERHR-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
- 229930040373 Paraformaldehyde Natural products 0.000 abstract 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 1
- 239000013543 active substance Substances 0.000 abstract 1
- 125000004442 acylamino group Chemical group 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- -1 analgesic Substances 0.000 abstract 1
- 230000000202 analgesic effect Effects 0.000 abstract 1
- 239000002260 anti-inflammatory agent Substances 0.000 abstract 1
- 230000001741 anti-phlogistic effect Effects 0.000 abstract 1
- 230000001754 anti-pyretic effect Effects 0.000 abstract 1
- 239000002221 antipyretic Substances 0.000 abstract 1
- 229940124630 bronchodilator Drugs 0.000 abstract 1
- 230000001813 broncholytic effect Effects 0.000 abstract 1
- 230000002425 cardiocirculatory effect Effects 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- WBJINCZRORDGAQ-UHFFFAOYSA-N formic acid ethyl ester Natural products CCOC=O WBJINCZRORDGAQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 229920002866 paraformaldehyde Polymers 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000000546 pharmaceutical excipient Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/34—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Rheumatology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Pain & Pain Management (AREA)
- Hospice & Palliative Care (AREA)
- Pulmonology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Hydrogenated Pyridines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
- Pyrrole Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT1178769A AT305987B (de) | 1969-12-18 | 1969-12-18 | Verfahren zur Herstellung von neuen Aminoketonen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1332930A true GB1332930A (en) | 1973-10-10 |
Family
ID=3630679
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB6019370A Expired GB1332930A (en) | 1969-12-18 | 1970-12-18 | Acyl derivatives of substituted bis-arylalklamines |
Country Status (16)
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4276307A (en) | 1980-01-25 | 1981-06-30 | Shell Oil Company | N-Phenethylaminopropiophenones as lipogenesis inhibitors |
| US4279925A (en) | 1980-01-25 | 1981-07-21 | Shell Oil Company | N-Phenethylaminopropiophenones as lipogenesis inhibitors |
| US4279929A (en) | 1980-01-25 | 1981-07-21 | Shell Oil Company | N-Phenethylaminopropiophenones as lipogenesis inhibitors |
| US4285970A (en) | 1980-01-25 | 1981-08-25 | Shell Oil Company | N-Phenethylaminopropiophenones as lipogenesis inhibitors |
| US4305960A (en) | 1980-01-25 | 1981-12-15 | Shell Oil Company | N-Phenethylaminopropiophenones as lipogenesis inhibitors |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL156669A0 (en) | 2003-06-26 | 2004-01-04 | Neurim Pharma 1991 | 2-aminobenzoyl derivatives |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL6609318A (enrdf_load_stackoverflow) * | 1966-07-04 | 1968-01-05 |
-
1969
- 1969-12-18 AT AT1178769A patent/AT305987B/de not_active IP Right Cessation
-
1970
- 1970-11-26 ES ES385918A patent/ES385918A1/es not_active Expired
- 1970-12-02 ZA ZA708151A patent/ZA708151B/xx unknown
- 1970-12-02 YU YU2927/70A patent/YU35434B/xx unknown
- 1970-12-08 NL NL7017884.A patent/NL164552C/xx not_active IP Right Cessation
- 1970-12-10 FI FI3330/70A patent/FI53700C/fi active
- 1970-12-15 CH CH1859570A patent/CH566963A5/xx not_active IP Right Cessation
- 1970-12-15 CH CH1342873A patent/CH566289A5/xx not_active IP Right Cessation
- 1970-12-15 CH CH1342773A patent/CH566288A5/xx not_active IP Right Cessation
- 1970-12-15 CH CH1342973A patent/CH566290A5/xx not_active IP Right Cessation
- 1970-12-16 SU SU1740985A patent/SU507224A3/ru active
- 1970-12-16 DE DE2061864A patent/DE2061864C3/de not_active Expired
- 1970-12-16 SU SU1499482A patent/SU470108A3/ru active
- 1970-12-16 SE SE7017064A patent/SE383874B/xx unknown
- 1970-12-16 SU SU1740556A patent/SU493956A3/ru active
- 1970-12-17 DK DK642170AA patent/DK137380B/da unknown
- 1970-12-17 BE BE760505A patent/BE760505A/xx unknown
- 1970-12-18 FR FR7045775A patent/FR2081381B1/fr not_active Expired
- 1970-12-18 CA CA101,047A patent/CA992979A/en not_active Expired
- 1970-12-18 GB GB6019370A patent/GB1332930A/en not_active Expired
- 1970-12-18 JP JP45114020A patent/JPS5245701B1/ja active Pending
-
1971
- 1971-09-18 ES ES395209A patent/ES395209A1/es not_active Expired
- 1971-09-18 ES ES395207A patent/ES395207A1/es not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4276307A (en) | 1980-01-25 | 1981-06-30 | Shell Oil Company | N-Phenethylaminopropiophenones as lipogenesis inhibitors |
| US4279925A (en) | 1980-01-25 | 1981-07-21 | Shell Oil Company | N-Phenethylaminopropiophenones as lipogenesis inhibitors |
| US4279929A (en) | 1980-01-25 | 1981-07-21 | Shell Oil Company | N-Phenethylaminopropiophenones as lipogenesis inhibitors |
| US4285970A (en) | 1980-01-25 | 1981-08-25 | Shell Oil Company | N-Phenethylaminopropiophenones as lipogenesis inhibitors |
| US4305960A (en) | 1980-01-25 | 1981-12-15 | Shell Oil Company | N-Phenethylaminopropiophenones as lipogenesis inhibitors |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |