ES265401A1 - Un procedimiento para preparar derivados sustituidos por nitrëgeno - Google Patents
Un procedimiento para preparar derivados sustituidos por nitrëgenoInfo
- Publication number
- ES265401A1 ES265401A1 ES0265401A ES265401A ES265401A1 ES 265401 A1 ES265401 A1 ES 265401A1 ES 0265401 A ES0265401 A ES 0265401A ES 265401 A ES265401 A ES 265401A ES 265401 A1 ES265401 A1 ES 265401A1
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- aryl
- phenyl
- general formula
- hydrogen atoms
- 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
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- -1 C1-6 alkyl sulphate Chemical compound 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 125000005843 halogen group Chemical group 0.000 abstract 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- 239000004202 carbamide Substances 0.000 abstract 2
- 235000013877 carbamide Nutrition 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical class OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 abstract 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 abstract 2
- WDGCBNTXZHJTHJ-UHFFFAOYSA-N 2h-1,3-oxazol-2-id-4-one Chemical compound O=C1CO[C-]=N1 WDGCBNTXZHJTHJ-UHFFFAOYSA-N 0.000 abstract 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 abstract 1
- 150000007945 N-acyl ureas Chemical class 0.000 abstract 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 abstract 1
- 229940100198 alkylating agent Drugs 0.000 abstract 1
- 239000002168 alkylating agent Substances 0.000 abstract 1
- 230000002152 alkylating effect Effects 0.000 abstract 1
- 230000029936 alkylation Effects 0.000 abstract 1
- 238000005804 alkylation reaction Methods 0.000 abstract 1
- 239000002269 analeptic agent Substances 0.000 abstract 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 abstract 1
- 239000002775 capsule Substances 0.000 abstract 1
- 235000015218 chewing gum Nutrition 0.000 abstract 1
- 229940112822 chewing gum Drugs 0.000 abstract 1
- 235000019219 chocolate Nutrition 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 235000009508 confectionery Nutrition 0.000 abstract 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 abstract 1
- 239000008298 dragée Substances 0.000 abstract 1
- 239000006196 drop Substances 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 230000032050 esterification Effects 0.000 abstract 1
- 238000005886 esterification reaction Methods 0.000 abstract 1
- JIZKCEDJMYWSLA-UHFFFAOYSA-N ethyl 2-(2-fluorophenyl)-2-hydroxyacetate Chemical compound CCOC(=O)C(O)C1=CC=CC=C1F JIZKCEDJMYWSLA-UHFFFAOYSA-N 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 238000011065 in-situ storage Methods 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 101150009274 nhr-1 gene Proteins 0.000 abstract 1
- 231100000252 nontoxic Toxicity 0.000 abstract 1
- 230000003000 nontoxic effect Effects 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000000546 pharmaceutical excipient Substances 0.000 abstract 1
- 229940124531 pharmaceutical excipient Drugs 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 1
- 239000000829 suppository Substances 0.000 abstract 1
- 239000000725 suspension Substances 0.000 abstract 1
- 235000020357 syrup Nutrition 0.000 abstract 1
- 239000006188 syrup Substances 0.000 abstract 1
- 239000003826 tablet Substances 0.000 abstract 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D263/46—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D263/48—Nitrogen atoms not forming part of a nitro radical
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3511560A | 1960-06-10 | 1960-06-10 | |
| US3511660A | 1960-06-10 | 1960-06-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES265401A1 true ES265401A1 (es) | 1961-09-01 |
Family
ID=26711766
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0265401A Expired ES265401A1 (es) | 1960-06-10 | 1961-03-04 | Un procedimiento para preparar derivados sustituidos por nitrëgeno |
Country Status (6)
| Country | Link |
|---|---|
| AT (1) | AT256101B (en(2012)) |
| CH (4) | CH437293A (en(2012)) |
| DK (2) | DK102861C (en(2012)) |
| ES (1) | ES265401A1 (en(2012)) |
| FR (1) | FR1555453A (en(2012)) |
| GB (1) | GB907848A (en(2012)) |
-
1961
- 1961-02-23 GB GB662561A patent/GB907848A/en not_active Expired
- 1961-03-03 FR FR1555453D patent/FR1555453A/fr not_active Expired
- 1961-03-04 ES ES0265401A patent/ES265401A1/es not_active Expired
- 1961-03-06 DK DK97861A patent/DK102861C/da active
- 1961-03-06 DK DK168762A patent/DK105405C/da active
- 1961-03-06 CH CH1536765A patent/CH437293A/de unknown
- 1961-03-06 CH CH264661A patent/CH401057A/de unknown
- 1961-03-06 CH CH264561A patent/CH413840A/de unknown
- 1961-03-06 AT AT656464A patent/AT256101B/de active
- 1961-03-06 CH CH1314365A patent/CH421965A/de unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DK102861C (da) | 1965-10-18 |
| FR1555453A (en(2012)) | 1969-01-31 |
| DK105405C (da) | 1966-09-26 |
| CH401057A (de) | 1965-10-31 |
| AT256101B (de) | 1967-08-10 |
| CH421965A (de) | 1966-10-15 |
| CH413840A (de) | 1966-05-31 |
| CH437293A (de) | 1967-06-15 |
| GB907848A (en) | 1962-10-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ATE107922T1 (de) | 2-(1-piperazinyl)-4-phenylcycloalkanpyridin- derivate, verfahren zu deren herstellung und pharmazeutische zusammensetzungen, die sie enthalten. | |
| ATE63124T1 (de) | Prodrugverbindungen, verfahren zu deren herstellung und diese enthaltende zubereitungen mit verzoegerter freisetzung. | |
| US2951843A (en) | Tetrahydrosoquinoline biguanides | |
| GB973361A (en) | Pyrazolo-pyrimidines and process for their manufacture | |
| ATE59033T1 (de) | N-enthaltende heterozyklische verbindungen, verfahren zu deren herstellung und diese enthaltende arzneimittel. | |
| GB989013A (en) | New guanidines and process for their manufacture | |
| ATE19773T1 (de) | Nitroaliphatische verbindungen, verfahren zu deren herstellung und deren verwendung. | |
| US3894039A (en) | 1-Halophenyl-2-imino-imidazolidines | |
| GB962293A (en) | New sydnonimines and process for their manufacture | |
| US2636891A (en) | Heterocyclic organo-tin compounds containing oxygen, sulfur, and tin in the ring | |
| ES265401A1 (es) | Un procedimiento para preparar derivados sustituidos por nitrëgeno | |
| US2742464A (en) | Production of capillary active amine-amides | |
| JPS5535067A (en) | Novel urea derivative and its preparation | |
| ES266788A1 (es) | Un procedimiento de preparar un derivado de 8-bencil dialcohil xantina | |
| GB1272337A (en) | New basic carbamates and preparation thereof | |
| US3773767A (en) | N-(hydroxy-or methoxy-alkyl)-2-(n'-(hydroxy or methoxy-alkyl)-phenyl-amino)-imidazolines-(2) and salts thereof | |
| GB824536A (en) | Improvements in or relating to new phenthiazine derivatives and processes for their preparation | |
| CH505072A (de) | Verfahren zur Herstellung von Sulfonylharnstoffderivaten | |
| GB850483A (en) | Improvements in or relating to pyrimidine derivatives | |
| ATE52509T1 (de) | Thiazolidinderivate und verfahren zu ihrer herstellung. | |
| GB1003889A (en) | Guanidines and isothioureas | |
| DE1001676B (de) | Verfahren zur Herstellung von Kondensationsprodukten | |
| ES262653A1 (es) | Un procedimiento para la preparaciën de compuestos terapeuticos | |
| GB927288A (en) | 1-and 7-(basically-substituted-alkyl) xanthine derivatives, a process for their manufacture and pharmaceutical compositions containing them | |
| GB823338A (en) | Diquaternary salts of aminoalkyl piperidines |