GB899556A - Substituted isonicotinic acid amides and process for their manufacture - Google Patents
Substituted isonicotinic acid amides and process for their manufactureInfo
- Publication number
- GB899556A GB899556A GB20266/59A GB2026659A GB899556A GB 899556 A GB899556 A GB 899556A GB 20266/59 A GB20266/59 A GB 20266/59A GB 2026659 A GB2026659 A GB 2026659A GB 899556 A GB899556 A GB 899556A
- Authority
- GB
- United Kingdom
- Prior art keywords
- isonicotinic acid
- propylamine
- diphenyl
- reacting
- formula
- 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
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
- C07D213/81—Amides; Imides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyridine Compounds (AREA)
Abstract
The invention comprises compounds of the formula <FORM:0899556/IV (b)/1> wherein R1 is a halogen atom or a methyl or methoxy group, R2 and R3 are hydrogen or halogen atoms, and R4 is a halogen atom) and their preparation by reacting isonicotinic acid or a reactive derivative thereof with the appropriately substituted 2,3-diphenyl-propylamine. Suitable reactive derivatives include halides and esters of isonicotinic acid, or the process may be effected by heating the salt of isonicotinic acid with the diphenyl-propylamine at 270 DEG C.-320 DEG C. until no more water is split off. Examples are given. Starting materials of the formula <FORM:0899556/IV (b)/2> are prepared by reacting an appropriately substituted benzaldehyde or benzyl halide, in the presence of an alkaline condensing agent, with a substituted benzyl cyanide and then reducing the products. The amides of the invention, which are stated to be cytostatic agents, may be formulated as pharmaceutical preparations with suitable carriers. Tablets, capsules, dragees, ampoules, solutions and suspensions are referred to, and these may contain stabilizers, buffers, wetting agents, emulsifiers or salts for regulating the osmotic pressure.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEF25947A DE1223388B (en) | 1958-06-12 | 1958-06-12 | Process for the preparation of new isonicotinic acid amides |
Publications (1)
Publication Number | Publication Date |
---|---|
GB899556A true GB899556A (en) | 1962-06-27 |
Family
ID=7091829
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB20266/59A Expired GB899556A (en) | 1958-06-12 | 1959-06-12 | Substituted isonicotinic acid amides and process for their manufacture |
Country Status (4)
Country | Link |
---|---|
BE (1) | BE579630A (en) |
CH (1) | CH375357A (en) |
DE (1) | DE1223388B (en) |
GB (1) | GB899556A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003087037A1 (en) * | 2002-04-05 | 2003-10-23 | Merck & Co., Inc. | Substituted aryl amides |
US7348456B2 (en) | 2002-12-19 | 2008-03-25 | Merck & Co., Inc. | Substituted amides |
-
1958
- 1958-06-12 DE DEF25947A patent/DE1223388B/en active Pending
-
1959
- 1959-06-10 CH CH7425459A patent/CH375357A/en unknown
- 1959-06-12 GB GB20266/59A patent/GB899556A/en not_active Expired
- 1959-06-12 BE BE579630A patent/BE579630A/en unknown
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003087037A1 (en) * | 2002-04-05 | 2003-10-23 | Merck & Co., Inc. | Substituted aryl amides |
US7348456B2 (en) | 2002-12-19 | 2008-03-25 | Merck & Co., Inc. | Substituted amides |
US7576239B2 (en) | 2002-12-19 | 2009-08-18 | Merck & Co., Inc. | Substituted amides |
Also Published As
Publication number | Publication date |
---|---|
CH375357A (en) | 1964-02-29 |
BE579630A (en) | 1959-12-14 |
DE1223388B (en) | 1966-08-25 |
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