IE41550L - Benzylpiperazine derivatives - Google Patents
Benzylpiperazine derivativesInfo
- Publication number
- IE41550L IE41550L IE751332A IE133275A IE41550L IE 41550 L IE41550 L IE 41550L IE 751332 A IE751332 A IE 751332A IE 133275 A IE133275 A IE 133275A IE 41550 L IE41550 L IE 41550L
- Authority
- IE
- Ireland
- Prior art keywords
- formula
- alkyl
- compound
- prepared
- derivatives
- Prior art date
Links
- IQXXEPZFOOTTBA-UHFFFAOYSA-N 1-benzylpiperazine Chemical class C=1C=CC=CC=1CN1CCNCC1 IQXXEPZFOOTTBA-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 238000006243 chemical reaction Methods 0.000 abstract 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- 150000002148 esters Chemical class 0.000 abstract 2
- 125000000524 functional group Chemical group 0.000 abstract 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 abstract 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 abstract 1
- -1 CF 3 Inorganic materials 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 abstract 1
- 230000001773 anti-convulsant effect Effects 0.000 abstract 1
- 239000001961 anticonvulsive agent Substances 0.000 abstract 1
- 229960003965 antiepileptics Drugs 0.000 abstract 1
- 239000002585 base Substances 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- PCOXUBXGOBQZIG-UHFFFAOYSA-N diethyl 2-[[2-(dimethylamino)acetyl]amino]propanedioate Chemical compound CCOC(=O)C(C(=O)OCC)NC(=O)CN(C)C PCOXUBXGOBQZIG-UHFFFAOYSA-N 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 235000019253 formic acid Nutrition 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 230000026030 halogenation Effects 0.000 abstract 1
- 238000005658 halogenation reaction Methods 0.000 abstract 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 238000007911 parenteral administration Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 238000010561 standard procedure Methods 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
-
- 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
- A61P25/08—Antiepileptics; Anticonvulsants
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
1476116 Triazole derivatives CIBA-GEIGY AG 9 June 1975 [14 June 1974] 24616/75 Heading C2C Novel compounds of Formula I wherein R 1 is H, C 1-7 alkyl, hydroxymethyl optionally etherified or esterified, formyl, carboxy optionally functionally modified, or aminomethyl optionally mono or disubstituted; B 2 is C 1-7 alkyl and R 3 is H or C 1-2 alkyl or NH 2 R 3 is a saturated monoheterocyclic ring and rings A and B may be substituted by halogen, CF 3 , NO 2 , C 1-7 alkyl or C 1-7 alkoxy and salts thereof are prepared by one of the following methods: (a) a reactive ester of a compound of Formula II is reacted with HNR 2 R 3 or an alkali metal derivative thereof; (b) a compound of Formula IV is reacted with formaldehyde or formic acid; (c) a compound of Formula V is oxidized; (d) a compound of Formula VI wherein R 6 is C 1-7 alkyl is treated with a base and optional conversion to a salt or a substituent group is converted to a derivative thereof by standard procedures. Reaction esters (mainly halides) of compounds of Formula II above are prepared by halogenation and optional conversion of functional groups to their derivatives. Intermediates of Formula V are prepared by NaBH 4 reduction of the ketones optionally followed by conversion of functional group to their derivatives. [2 - (Dimethylamino) - acetamido] - [2 - (ochlorobenzoyl) - 4 - chlorophenylazo] - malonic acid diethyl ester is prepared by reacting 2- amino - 2<SP>1</SP>,5 - dichlorobenzophenone which has been diazotized with [2-(dimethylamino)acetamido]-malonic acid diethyl ester. Pharmaceutical compositions in conventional forms for oral, rectal or parenteral administration and having anticonvulsant activity comprise an above novel compound and a carrier or diluent.
[GB1476116A]
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH817574A CH601264A5 (en) | 1974-06-14 | 1974-06-14 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IE41550L true IE41550L (en) | 1975-12-14 |
| IE41550B1 IE41550B1 (en) | 1980-01-30 |
Family
ID=4336312
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IE1332/75A IE41550B1 (en) | 1974-06-14 | 1975-06-13 | New triazole derivatives and process for the production thereof |
Country Status (22)
| Country | Link |
|---|---|
| JP (3) | JPS6028825B2 (en) |
| AT (2) | AT345821B (en) |
| AU (1) | AU496929B2 (en) |
| BE (1) | BE830214A (en) |
| CA (1) | CA1074313A (en) |
| CH (1) | CH601264A5 (en) |
| CS (1) | CS189712B2 (en) |
| DE (1) | DE2525691A1 (en) |
| DK (1) | DK227075A (en) |
| DO (1) | DOP1980002934A (en) |
| ES (4) | ES438481A1 (en) |
| FR (1) | FR2274302A1 (en) |
| GB (1) | GB1476116A (en) |
| GT (1) | GT198066871A (en) |
| HK (1) | HK49580A (en) |
| HU (1) | HU172467B (en) |
| IE (1) | IE41550B1 (en) |
| IL (1) | IL47474A (en) |
| MY (1) | MY8100158A (en) |
| NL (1) | NL7507104A (en) |
| SE (1) | SE426393B (en) |
| ZA (1) | ZA753809B (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5855147B2 (en) * | 1976-06-04 | 1983-12-08 | 塩野義製薬株式会社 | benzophenone derivatives |
| CN113372215B (en) * | 2021-05-20 | 2024-05-24 | 吉林大学 | Novel esterification method for synthesizing p-halomethyl benzoate |
| WO2023052312A1 (en) | 2021-09-29 | 2023-04-06 | F. Hoffmann-La Roche Ag | New benzodiazepine derivatives as gaba a gamma1 pam |
-
1974
- 1974-06-14 CH CH817574A patent/CH601264A5/xx not_active IP Right Cessation
-
1975
- 1975-05-23 DK DK227075A patent/DK227075A/en not_active Application Discontinuation
- 1975-05-26 SE SE7505952A patent/SE426393B/en not_active IP Right Cessation
- 1975-06-09 GB GB2461675A patent/GB1476116A/en not_active Expired
- 1975-06-10 DE DE19752525691 patent/DE2525691A1/en not_active Ceased
- 1975-06-11 FR FR7518236A patent/FR2274302A1/en active Granted
- 1975-06-12 ES ES438481A patent/ES438481A1/en not_active Expired
- 1975-06-12 CA CA229,230A patent/CA1074313A/en not_active Expired
- 1975-06-12 IL IL7547474A patent/IL47474A/en unknown
- 1975-06-12 AU AU82082/75A patent/AU496929B2/en not_active Expired
- 1975-06-13 BE BE157308A patent/BE830214A/en not_active IP Right Cessation
- 1975-06-13 AT AT455875A patent/AT345821B/en not_active IP Right Cessation
- 1975-06-13 IE IE1332/75A patent/IE41550B1/en unknown
- 1975-06-13 NL NL7507104A patent/NL7507104A/en not_active Application Discontinuation
- 1975-06-13 HU HU75CI00001590A patent/HU172467B/en unknown
- 1975-06-13 CS CS754192A patent/CS189712B2/en unknown
- 1975-06-13 ZA ZA00753809A patent/ZA753809B/en unknown
- 1975-06-14 JP JP7571466A patent/JPS6028825B2/en not_active Expired
-
1976
- 1976-12-06 ES ES454005A patent/ES454005A1/en not_active Expired
- 1976-12-06 ES ES454006A patent/ES454006A1/en not_active Expired
- 1976-12-06 ES ES454008A patent/ES454008A1/en not_active Expired
-
1977
- 1977-07-12 AT AT498877A patent/AT345822B/en not_active IP Right Cessation
-
1980
- 1980-09-04 HK HK495/80A patent/HK49580A/en unknown
- 1980-11-25 DO DO1980002934A patent/DOP1980002934A/en unknown
- 1980-12-12 GT GT198066871A patent/GT198066871A/en unknown
-
1981
- 1981-12-30 MY MY158/81A patent/MY8100158A/en unknown
-
1983
- 1983-11-25 JP JP58220864A patent/JPS59108770A/en active Granted
- 1983-11-25 JP JP58220863A patent/JPS6021984B2/en not_active Expired
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