CH534129A - (A) Cmpds. of general formula (I):- A = N or CH R = H or Me R' = (1-4 C) alkyl, (1-4C) alkylO-, NO2, CF3, or halogen R2 and R3 = H, halo - Google Patents
(A) Cmpds. of general formula (I):- A = N or CH R = H or Me R' = (1-4 C) alkyl, (1-4C) alkylO-, NO2, CF3, or halogen R2 and R3 = H, haloInfo
- Publication number
- CH534129A CH534129A CH945370A CH945370A CH534129A CH 534129 A CH534129 A CH 534129A CH 945370 A CH945370 A CH 945370A CH 945370 A CH945370 A CH 945370A CH 534129 A CH534129 A CH 534129A
- Authority
- CH
- Switzerland
- Prior art keywords
- halogen
- alkyl
- cmpds
- alkylo
- general formula
- Prior art date
Links
- 125000000217 alkyl group Chemical group 0.000 title abstract 3
- 229910052736 halogen Inorganic materials 0.000 title abstract 3
- 150000002367 halogens Chemical class 0.000 title abstract 3
- 125000001475 halogen functional group Chemical group 0.000 title 1
- SWYJYGCPTGKBDS-UHFFFAOYSA-N 2,3-dihydroxypropyl 2-(3-chloro-2-methylanilino)pyridine-3-carboxylate Chemical compound CC1=C(Cl)C=CC=C1NC1=NC=CC=C1C(=O)OCC(O)CO SWYJYGCPTGKBDS-UHFFFAOYSA-N 0.000 abstract 1
- 150000001241 acetals Chemical class 0.000 abstract 1
- 229940035676 analgesics Drugs 0.000 abstract 1
- 239000000730 antalgic agent Substances 0.000 abstract 1
- 239000002260 anti-inflammatory agent Substances 0.000 abstract 1
- 229940121363 anti-inflammatory agent Drugs 0.000 abstract 1
- 230000003110 anti-inflammatory effect Effects 0.000 abstract 1
- 230000001754 anti-pyretic effect Effects 0.000 abstract 1
- 239000002221 antipyretic Substances 0.000 abstract 1
- 229940125716 antipyretic agent Drugs 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/79—Acids; Esters
- C07D213/80—Acids; Esters in position 3
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
(A) Cmpds. of general formula (I):- A = N or CH R = H or Me R' = (1-4 C) alkyl, (1-4C) alkylO-, NO2, CF3, or halogen R2 and R3 = H, halogen, (1-4C) alkyl, NO2 or CF3 (B) Acetals and ketals of (I) (C) Salts of (I) and (B). Anti-inflammatories, antipyretics, and analgesics. glyceryl-2-(2-methyl-3-chloroanilino)nicotinate, m.p. 113-4 deg.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH945370A CH534129A (en) | 1968-04-04 | 1968-04-04 | (A) Cmpds. of general formula (I):- A = N or CH R = H or Me R' = (1-4 C) alkyl, (1-4C) alkylO-, NO2, CF3, or halogen R2 and R3 = H, halo |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH945370A CH534129A (en) | 1968-04-04 | 1968-04-04 | (A) Cmpds. of general formula (I):- A = N or CH R = H or Me R' = (1-4 C) alkyl, (1-4C) alkylO-, NO2, CF3, or halogen R2 and R3 = H, halo |
| CH502968A CH534130A (en) | 1967-04-10 | 1968-04-04 | Process for the preparation of new, pharmacologically active nicotinic and anthranilic acid derivatives and of intermediates for the preparation of these active compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH534129A true CH534129A (en) | 1973-02-28 |
Family
ID=4286721
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH945370A CH534129A (en) | 1968-04-04 | 1968-04-04 | (A) Cmpds. of general formula (I):- A = N or CH R = H or Me R' = (1-4 C) alkyl, (1-4C) alkylO-, NO2, CF3, or halogen R2 and R3 = H, halo |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH534129A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP4021449A4 (en) * | 2019-08-30 | 2023-11-01 | University of South Florida | STING MODULATORS, COMPOSITIONS AND METHODS OF USE |
-
1968
- 1968-04-04 CH CH945370A patent/CH534129A/en not_active IP Right Cessation
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP4021449A4 (en) * | 2019-08-30 | 2023-11-01 | University of South Florida | STING MODULATORS, COMPOSITIONS AND METHODS OF USE |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |