SE8206445L - ANALOGY PROCEDURE FOR THE PREPARATION OF THERAPEUTICALLY ACTIVE DI-N-PROPYLMethylamine derivatives - Google Patents
ANALOGY PROCEDURE FOR THE PREPARATION OF THERAPEUTICALLY ACTIVE DI-N-PROPYLMethylamine derivativesInfo
- Publication number
- SE8206445L SE8206445L SE8206445A SE8206445A SE8206445L SE 8206445 L SE8206445 L SE 8206445L SE 8206445 A SE8206445 A SE 8206445A SE 8206445 A SE8206445 A SE 8206445A SE 8206445 L SE8206445 L SE 8206445L
- Authority
- SE
- Sweden
- Prior art keywords
- preparation
- acid addition
- derivatives
- propyl
- reacted
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D203/00—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom
- C07D203/04—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D203/06—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D203/08—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring nitrogen atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
- C07D295/027—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring
- C07D295/03—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring with the ring nitrogen atoms directly attached to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/14—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D295/145—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/15—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
(21)Ans nr 8206445-2 Rotel 8206 (51)Klass C 07 0 205/04 C 07 0 203/08 (74)0mbud HArne Patentkrav van i R och n har samma betydelse som oven, eller med ett syraadditionssalt av deems firening, corn ger det Onskade metylaminderivatet som sedan kan reageras med Wagon organisk eller oorganisk syra till ett farmaceutiskt godtagbart syraadditionssalt av derivatet. 1. Analogiforfarande fir framstallning av nya di-n-propyl-metylaminderivat med den generella formeln RC-N(C112)fl /rn-C3R, och de farmaceutiskt godtagbara syraadditionssalterna darav, vani R betecknar n-propyl, isopropyl, isobutyl eller allyl och n an 0 eller 1,kHnnetecknatav au t ett lampligt cykliseringsmedel reageras i ett losningsmedel eller i franvaro av nagot losningsmedel med en alkohol med den generella formeln: RC-NH-C112-110CH2OH n-030 II (21) Ans nr 8206445-2 Rotel 8206 (51) Klass C 07 0 205/04 C 07 0 203/08 (74) 0mbud HArne , corn gives the desired methylamine derivative which can then be reacted with Wagon organic or inorganic acid to form a pharmaceutically acceptable acid addition salt of the derivative. An analogous process for the preparation of novel di-n-propyl-methylamine derivatives of the general formula RC-N (C112) fl / rn-C3R, and the pharmaceutically acceptable acid addition salts thereof, vani R represents n-propyl, isopropyl, isobutyl or allyl and n 0 or 1, the characteristic sign of a suitable cyclizing agent is reacted in a solvent or in the absence of any solvent with an alcohol of the general formula: RC-NH-C112-110CH 2 OH n-030 II
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE842528 | 1976-06-03 |
Publications (3)
Publication Number | Publication Date |
---|---|
SE8206445L true SE8206445L (en) | 1982-11-12 |
SE8206445D0 SE8206445D0 (en) | 1982-11-12 |
SE452763B SE452763B (en) | 1987-12-14 |
Family
ID=3861370
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE7706448A SE452317B (en) | 1976-06-03 | 1977-06-02 | ANALOGY PROCEDURE FOR THE PREPARATION OF THERAPEUTICALLY ACTIVE, NEW DI-N-PROPYL-METHYLAMINE DERIVATIVES |
SE8206445A SE452763B (en) | 1976-06-03 | 1982-11-12 | ANALOGY PROCEDURE FOR THE PREPARATION OF THERAPEUTICALLY ACTIVE DI-N-PROPYL-METHYLAMINE DERIVATIVES |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE7706448A SE452317B (en) | 1976-06-03 | 1977-06-02 | ANALOGY PROCEDURE FOR THE PREPARATION OF THERAPEUTICALLY ACTIVE, NEW DI-N-PROPYL-METHYLAMINE DERIVATIVES |
Country Status (17)
Country | Link |
---|---|
JP (1) | JPS6039261B2 (en) |
AR (4) | AR213646A1 (en) |
AT (1) | AT352088B (en) |
AU (1) | AU511705B2 (en) |
DK (1) | DK146063C (en) |
ES (2) | ES459466A1 (en) |
FI (1) | FI63015C (en) |
FR (2) | FR2374901A1 (en) |
GR (1) | GR61148B (en) |
MX (1) | MX4778E (en) |
NL (1) | NL7706052A (en) |
NO (1) | NO145337C (en) |
NZ (1) | NZ184161A (en) |
PT (1) | PT66623B (en) |
SE (2) | SE452317B (en) |
YU (1) | YU129577A (en) |
ZA (1) | ZA773151B (en) |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE815273A (en) * | 1974-05-20 | 1974-11-20 | METHYLAMINE ACTIVE DERIVATIVES | |
BE842528R (en) * | 1976-06-03 | 1976-12-03 | METHYLAMINE ACTIVE DERIVATIVES, THERAPEUTIC COMPOSITIONS CONTAINING THEM AND THE PROCESSES FOR THE PREPARATION OF THESE DERIVATIVES AND COMPOSITIONS |
-
1977
- 1977-05-14 GR GR53468A patent/GR61148B/en unknown
- 1977-05-20 NZ NZ184161A patent/NZ184161A/en unknown
- 1977-05-24 YU YU01295/77A patent/YU129577A/en unknown
- 1977-05-25 ZA ZA00773151A patent/ZA773151B/en unknown
- 1977-05-27 AU AU25561/77A patent/AU511705B2/en not_active Ceased
- 1977-05-27 FR FR7716280A patent/FR2374901A1/en active Granted
- 1977-06-02 DK DK244677A patent/DK146063C/en not_active IP Right Cessation
- 1977-06-02 NL NL7706052A patent/NL7706052A/en not_active Application Discontinuation
- 1977-06-02 SE SE7706448A patent/SE452317B/en not_active IP Right Cessation
- 1977-06-02 AR AR267925A patent/AR213646A1/en active
- 1977-06-02 PT PT66623A patent/PT66623B/en unknown
- 1977-06-02 NO NO771941A patent/NO145337C/en unknown
- 1977-06-03 AT AT395877A patent/AT352088B/en not_active IP Right Cessation
- 1977-06-03 ES ES459466A patent/ES459466A1/en not_active Expired
- 1977-06-03 FI FI771780A patent/FI63015C/en not_active IP Right Cessation
- 1977-06-03 MX MX775778U patent/MX4778E/en unknown
- 1977-06-03 JP JP52066217A patent/JPS6039261B2/en not_active Expired
-
1978
- 1978-03-21 FR FR7808094A patent/FR2372795A1/en active Granted
- 1978-04-26 AR AR271896A patent/AR215175A1/en active
- 1978-04-26 AR AR271895A patent/AR215052A1/en active
- 1978-04-26 AR AR271897A patent/AR215053A1/en active
- 1978-05-31 ES ES470379A patent/ES470379A1/en not_active Expired
-
1982
- 1982-11-12 SE SE8206445A patent/SE452763B/en not_active IP Right Cessation
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Legal Events
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NUG | Patent has lapsed |
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