ES421086A1 - Procedure for the preparation of new pigments of isoindolinone. (Machine-translation by Google Translate, not legally binding) - Google Patents
Procedure for the preparation of new pigments of isoindolinone. (Machine-translation by Google Translate, not legally binding)Info
- Publication number
- ES421086A1 ES421086A1 ES421086A ES421086A ES421086A1 ES 421086 A1 ES421086 A1 ES 421086A1 ES 421086 A ES421086 A ES 421086A ES 421086 A ES421086 A ES 421086A ES 421086 A1 ES421086 A1 ES 421086A1
- Authority
- ES
- Spain
- Prior art keywords
- atom
- isoindolinone
- formula
- group
- translation
- 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
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 2
- 239000000049 pigment Substances 0.000 title abstract 2
- 238000002360 preparation method Methods 0.000 title abstract 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 abstract 2
- 150000001342 alkaline earth metals Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000005115 alkyl carbamoyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000005116 aryl carbamoyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 abstract 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 125000000879 imine group Chemical group 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- -1 nitro, carbamoyl Chemical group 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
Landscapes
- Indole Compounds (AREA)
Abstract
Procedure for the preparation of new isoindolinone pigments, of the formula **(See formula)** in which M stands for a polyvalent, non-alkaline earth metal atom; R signifies an organic radical; X means an atom of 0 or S or an imine group X1 and Y1 signify hydrogen or halogen atoms, alkyl, alkoxy, alkoxycarbonyl, alkylsulfonyl or alkylcarbamoyl groups having 1 to 6 carbon atoms or groups of nitro, carbamoyl or arylcarbamoyl or together form a juxtacondensed benzene ring; X2 signifies a hydrogen atom; Y means a halogen atom; Z means a nitro group or a group of the formula R1Y2 (where R1 represents a hydrogen atom, an alkyl or cycloalkyl group provided with 1 to 6 carbon atoms or an aralkyl or aryl group and Y2 represents an atom of 0 or S); m is equal to 0-4; n equals 0-4; £ equals 0-3; and the sum of m + n + p must matter 4, characterized by reacting hot and in a solvent medium, preferably dimothylformamide or diethylene glycol monoethyl ether, an isoindolinone of the general formula **(See formula)** in which the substituents have the same meaning already described, with non-alkaline earth metal polyvalent assignment agents, in the form of preferably organic salts; Optionally, conducting by the single crucible system in the same isoindolinone-forming condensation medium. (Machine-translation by Google Translate, not legally binding)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1762572A CH580678A5 (en) | 1972-12-04 | 1972-12-04 | |
| CH1344573 | 1973-09-19 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES421086A1 true ES421086A1 (en) | 1976-08-01 |
Family
ID=25712322
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES421086A Expired ES421086A1 (en) | 1972-12-04 | 1973-12-03 | Procedure for the preparation of new pigments of isoindolinone. (Machine-translation by Google Translate, not legally binding) |
Country Status (2)
| Country | Link |
|---|---|
| ES (1) | ES421086A1 (en) |
| IT (1) | IT1003255B (en) |
-
1973
- 1973-11-30 IT IT3200173A patent/IT1003255B/en active
- 1973-12-03 ES ES421086A patent/ES421086A1/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| IT1003255B (en) | 1976-06-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| ES434345A1 (en) | Dyestuffs | |
| GB1437789A (en) | Cyclopropane derivatives and their use as pesticides | |
| GB1129072A (en) | Benzofuran and indole derivatives | |
| ES393496A1 (en) | Cerivatives of 2-pyrrolidinone | |
| ES429803A1 (en) | Azomethine pigments | |
| ES421086A1 (en) | Procedure for the preparation of new pigments of isoindolinone. (Machine-translation by Google Translate, not legally binding) | |
| GB1378127A (en) | Scopolamine derivatives | |
| ES428400A1 (en) | Pheno aldehydes | |
| ES450381A1 (en) | Indaneacetic acid derivatives | |
| SE7612685L (en) | PROCEDURE FOR PREPARING NEW IMIDAZOLE COMPOUNDS | |
| ES485361A1 (en) | PROCEDURE FOR PREPARING PIRROLIDINE DERIVATIVES | |
| SE7714017L (en) | EPOXIDE HARD MIXTURES | |
| ES440575A1 (en) | Manufacture of novel propylene-diamine derivative | |
| ES8100258A1 (en) | Chromogenic propenylenesulfone compounds | |
| ES426427A1 (en) | A PROCEDURE FOR THE PREPARATION OF NEW DENITROCARBOSTIRILE DERIVATIVES. | |
| ES419439A1 (en) | Carbamoyl sulphoxides | |
| ES382883A1 (en) | Water-insoluble phenyl-azo-naphthyl-amido-benzimidazolone dyestuffs | |
| ES411563A1 (en) | Coumarinimides | |
| SE7505272L (en) | NEW, NITROGENIC, POLYCYCLIC ASSOCIATIONS JUST SEE FOR THEIR PREPARATION. | |
| GB1317179A (en) | Diglycidyl derivatives of n-heterocyclic compounds processes for their manufacute and use | |
| ES435113A1 (en) | Azoquinolone pigments | |
| SE7712040L (en) | BIOLOGICALLY ACTIVE TRICYCLIC ASSOCIATIONS AND PROCEDURES FOR THEIR PREPARATION | |
| GB1331286A (en) | Diazonaphthalene compounds | |
| ES403237A1 (en) | Iminoisoindolinone dyestuffs and process for their manufacture | |
| ES416144A1 (en) | Procedure for the preparation of new polyglicidyl compounds containing N-heterocicles. (Machine-translation by Google Translate, not legally binding) |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FD1A | Patent lapsed |
Effective date: 19860210 |