GB741228A - Improvements in or relating to triazole compounds - Google Patents
Improvements in or relating to triazole compoundsInfo
- Publication number
- GB741228A GB741228A GB2877352A GB2877352A GB741228A GB 741228 A GB741228 A GB 741228A GB 2877352 A GB2877352 A GB 2877352A GB 2877352 A GB2877352 A GB 2877352A GB 741228 A GB741228 A GB 741228A
- Authority
- GB
- United Kingdom
- Prior art keywords
- mercapto
- allyl
- amino
- triazole
- guanidino
- 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
- -1 triazole compounds Chemical class 0.000 title 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 abstract 3
- 239000002585 base Substances 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 2
- PHKBWGVAGDUJIS-UHFFFAOYSA-N (diaminomethylideneamino)thiourea Chemical compound NC(=N)NNC(N)=S PHKBWGVAGDUJIS-UHFFFAOYSA-N 0.000 abstract 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- 229910002651 NO3 Inorganic materials 0.000 abstract 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 abstract 1
- 230000021736 acetylation Effects 0.000 abstract 1
- 238000006640 acetylation reaction Methods 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 238000006480 benzoylation reaction Methods 0.000 abstract 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 238000010992 reflux Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 150000003852 triazoles Chemical class 0.000 abstract 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/34—Fog-inhibitors; Stabilisers; Agents inhibiting latent image regression
- G03C1/346—Organic derivatives of bivalent sulfur, selenium or tellurium
-
- 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
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles 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
- C07D249/14—Nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention comprises substituted triazoles of the general tautomeric formul : <FORM:0741228/IV(a)/1> and the corresponding 3-acylamino compounds, wherein R represents an alkyl, alkenyl, aralkyl, cycloalkyl or aryl group; and a process for their preparation by treating a guanidino thiourea of formula R.NH.CS.NH.NH.C(NH2) : NH or acid salt thereof with a base, and thereafter acylating the product if the 3-acylamino derivatives are required. Specified bases are alkali metal hydroxides and carbonates, pyridine and triethylamine. In examples: (1) 4-ethyl - 3 - amino - 5 - mercapto - 4 : 1 : 2-triazole is prepared from N-ethyl-N1-guanidino thiouea hydrochloride, nitrate or acetate by refluxing with (a) sodium hydroxide solution, or (b) pyridine, and acidifying the product. The corresponding 4-methyl-, 4-iso-propyl-, 4-allyl-, 4-benzyl-, 4-cyclohexyl- and 4-phenyl-3 - amino - 5 - mercapto - 4 : 1 : 2 - triazoles are likewise obtained by method (a); (2) 4-allyl-3-acetamino- and 4-allyl-3-benzoylamino-5-mercapto-4 : 1 : 2-triazole are prepared by acetylation and benzoylation of the 3-amino compound. Specification 741,280 is referred to.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2877352A GB741228A (en) | 1952-11-14 | 1952-11-14 | Improvements in or relating to triazole compounds |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2877352A GB741228A (en) | 1952-11-14 | 1952-11-14 | Improvements in or relating to triazole compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB741228A true GB741228A (en) | 1955-11-30 |
Family
ID=10280919
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2877352A Expired GB741228A (en) | 1952-11-14 | 1952-11-14 | Improvements in or relating to triazole compounds |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB741228A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3189614A (en) * | 1960-08-16 | 1965-06-15 | Bellon Labor Sa Roger | 3-hydroxy-4-hydrocarbon-5-tertiary amino triazoles and process for their preparation |
| DE1222068B (en) * | 1960-08-16 | 1966-08-04 | Roger Bellon Fa Lab | Process for the preparation of trisubstituted 1, 2, 4-triazoles |
| US4281059A (en) | 1978-12-12 | 1981-07-28 | Konishiroku Photo Industry Co., Ltd. | Photographic material |
| EP0046871A1 (en) * | 1980-09-02 | 1982-03-10 | Agfa-Gevaert AG | Photographic material, process for its preparation, method for the production of photographic pictures as well as triazols |
-
1952
- 1952-11-14 GB GB2877352A patent/GB741228A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3189614A (en) * | 1960-08-16 | 1965-06-15 | Bellon Labor Sa Roger | 3-hydroxy-4-hydrocarbon-5-tertiary amino triazoles and process for their preparation |
| DE1222068B (en) * | 1960-08-16 | 1966-08-04 | Roger Bellon Fa Lab | Process for the preparation of trisubstituted 1, 2, 4-triazoles |
| US4281059A (en) | 1978-12-12 | 1981-07-28 | Konishiroku Photo Industry Co., Ltd. | Photographic material |
| EP0046871A1 (en) * | 1980-09-02 | 1982-03-10 | Agfa-Gevaert AG | Photographic material, process for its preparation, method for the production of photographic pictures as well as triazols |
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