SU429583A3 - - Google Patents
Info
- Publication number
- SU429583A3 SU429583A3 SU1495559A SU1495559A SU429583A3 SU 429583 A3 SU429583 A3 SU 429583A3 SU 1495559 A SU1495559 A SU 1495559A SU 1495559 A SU1495559 A SU 1495559A SU 429583 A3 SU429583 A3 SU 429583A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- phthalimido
- mol
- triazine
- phthalimide
- cyanuric chloride
- Prior art date
Links
- MGNCLNQXLYJVJD-UHFFFAOYSA-N cyanuric chloride Chemical compound ClC1=NC(Cl)=NC(Cl)=N1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- FYRHIOVKTDQVFC-UHFFFAOYSA-M potassium phthalimide Chemical compound [K+].C1=CC=C2C(=O)[N-]C(=O)C2=C1 FYRHIOVKTDQVFC-UHFFFAOYSA-M 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000001309 chloro group Chemical group Cl* 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- SPAZWLWQEDJMAW-UHFFFAOYSA-N 2-(4,6-dichloro-1,3,5-triazin-2-yl)isoindole-1,3-dione Chemical compound ClC1=NC(Cl)=NC(N2C(C3=CC=CC=C3C2=O)=O)=N1 SPAZWLWQEDJMAW-UHFFFAOYSA-N 0.000 description 1
- YXYAWRUGUHOBFC-UHFFFAOYSA-N 2-[4,6-bis(1,3-dioxoisoindol-2-yl)-1,3,5-triazin-2-yl]isoindole-1,3-dione Chemical compound O=C1C2=CC=CC=C2C(=O)N1C1=NC(N2C(C3=CC=CC=C3C2=O)=O)=NC(N2C(C3=CC=CC=C3C2=O)=O)=N1 YXYAWRUGUHOBFC-UHFFFAOYSA-N 0.000 description 1
- ILGOUVXDTDKOAN-UHFFFAOYSA-N 2-[4-chloro-6-(1,3-dioxoisoindol-2-yl)-1,3,5-triazin-2-yl]isoindole-1,3-dione Chemical compound O=C1C2=CC=CC=C2C(=O)N1C1=NC(N2C(C3=CC=CC=C3C2=O)=O)=NC(Cl)=N1 ILGOUVXDTDKOAN-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- -1 phthalimide alkali metal Chemical class 0.000 description 1
- 125000005544 phthalimido group Chemical group 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Priority Applications (13)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB5344070A GB1324718A (en) | 1970-11-10 | 1970-11-10 | Phthalimido triazines |
| CH1410574A CH564551A5 (enExample) | 1970-11-10 | 1970-11-12 | |
| CH1676070A CH557828A (de) | 1970-11-10 | 1970-11-12 | Verfahren zur herstellung substituierter phthalimido-1,3,5triazine. |
| CS74548A CS165317B2 (en) | 1970-11-10 | 1970-11-16 | Method of substituted phthalimide-1,3,5-triazines production |
| CS74547A CS165316B2 (en) | 1970-11-10 | 1970-11-16 | Method of substituted phthalimide-1,3,5-triazines production |
| SU1495559A SU429583A3 (enExample) | 1970-11-10 | 1970-11-17 | |
| SU701495559D SU452962A3 (ru) | 1970-11-10 | 1970-11-17 | Способ получени фталимидо-1,3,5триазинов |
| SU1766767A SU437297A1 (ru) | 1970-11-17 | Способ получени фталимидо-1,3,5-триазинов | |
| NL7017108A NL7017108A (enExample) | 1970-11-10 | 1970-11-23 | |
| FR7042588A FR2115622A5 (enExample) | 1970-11-10 | 1970-11-26 | |
| BE759524D BE759524A (en) | 1970-11-10 | 1970-11-27 | Herbicidal phthalimido - 1,3,5-triazine derivs |
| US00098026A US3794641A (en) | 1970-11-10 | 1970-12-14 | Substituted phthalimido-1,3,5-triazines |
| CH1676070A CH583210A5 (enExample) | 1970-11-10 | 1975-04-17 |
Applications Claiming Priority (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB5344070 | 1970-11-10 | ||
| CH1410574A CH564551A5 (enExample) | 1970-11-10 | 1970-11-12 | |
| CH1676070A CH557828A (de) | 1970-11-10 | 1970-11-12 | Verfahren zur herstellung substituierter phthalimido-1,3,5triazine. |
| CS74547A CS165316B2 (en) | 1970-11-10 | 1970-11-16 | Method of substituted phthalimide-1,3,5-triazines production |
| CS74548A CS165317B2 (en) | 1970-11-10 | 1970-11-16 | Method of substituted phthalimide-1,3,5-triazines production |
| SU1495559A SU429583A3 (enExample) | 1970-11-10 | 1970-11-17 | |
| SU1766767A SU437297A1 (ru) | 1970-11-17 | Способ получени фталимидо-1,3,5-триазинов | |
| NL7017108A NL7017108A (enExample) | 1970-11-10 | 1970-11-23 | |
| FR7042588A FR2115622A5 (enExample) | 1970-11-10 | 1970-11-26 | |
| BE759524 | 1970-11-27 | ||
| US9802670A | 1970-12-14 | 1970-12-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU429583A3 true SU429583A3 (enExample) | 1974-05-25 |
Family
ID=34109346
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU701495559D SU452962A3 (ru) | 1970-11-10 | 1970-11-17 | Способ получени фталимидо-1,3,5триазинов |
| SU1495559A SU429583A3 (enExample) | 1970-11-10 | 1970-11-17 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU701495559D SU452962A3 (ru) | 1970-11-10 | 1970-11-17 | Способ получени фталимидо-1,3,5триазинов |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3794641A (enExample) |
| BE (1) | BE759524A (enExample) |
| CH (3) | CH564551A5 (enExample) |
| CS (2) | CS165317B2 (enExample) |
| FR (1) | FR2115622A5 (enExample) |
| GB (1) | GB1324718A (enExample) |
| NL (1) | NL7017108A (enExample) |
| SU (2) | SU452962A3 (enExample) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3896224A (en) * | 1972-04-10 | 1975-07-22 | Ciba Geigy Corp | 1-(4',6'-dichloro-s-triazin-2-ylcarbamoyl)-2-methoxy- carbonylamino-benzimidazole |
| AU2316897A (en) * | 1996-03-01 | 1997-09-16 | Cytec Technology Corp. | Cyclic imido-1,3,5-triazine crosslinking agents |
| EP1389203B8 (en) * | 2001-02-27 | 2010-03-10 | The Governement of the United States of America, represented by The Secretary Department of Health and Human services | Analogs of thalidomide as angiogenesis inhibitors |
| AT410797B (de) * | 2001-07-26 | 2003-07-25 | Agrolinz Melamin Gmbh | Imidotriazinderivate |
| WO2005028436A2 (en) * | 2003-09-17 | 2005-03-31 | The Government Of The United States Of America, As Represented By The Secretary Of The Department Of Health And Human Services | Thalidomide analogs as tnf-alpha modulators |
| US8952895B2 (en) | 2011-06-03 | 2015-02-10 | Apple Inc. | Motion-based device operations |
| CA2648216C (en) * | 2006-04-13 | 2016-06-07 | Michael Gutschow | Tetrahalogenated compounds useful as inhibitors of angiogenesis |
| KR20090043475A (ko) * | 2006-05-22 | 2009-05-06 | 뉴욕 유니버시티 | 증강된 ｔｈ-1 프로파일을 나타내는 ｃ-당지질 |
| US8415470B2 (en) | 2011-06-24 | 2013-04-09 | E I Du Pont De Nemours And Company | Di-isoimide composition |
| US8536170B2 (en) | 2011-06-24 | 2013-09-17 | E I Du Pont De Nemours And Company | Curable composition comprising a di-isoimide, method of curing, and the cured composition so formed |
| US8586734B2 (en) | 2011-06-24 | 2013-11-19 | E I Du Pont De Nemours And Company | Process for preparing substituted and unsubstituted diamino triazine aromatic di-isoimides |
| US8927725B2 (en) | 2011-12-02 | 2015-01-06 | The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Thio compounds |
| CN105330650B (zh) * | 2015-11-04 | 2018-01-02 | 中北大学 | 一种非极性改性三聚氰胺基阻燃剂的制备方法及应用 |
| CN106866636B (zh) * | 2016-12-27 | 2019-09-03 | 中国石油天然气股份有限公司 | 一种亚酰胺类β晶型成核剂及其制备方法与应用 |
-
1970
- 1970-11-10 GB GB5344070A patent/GB1324718A/en not_active Expired
- 1970-11-12 CH CH1410574A patent/CH564551A5/de not_active IP Right Cessation
- 1970-11-12 CH CH1676070A patent/CH557828A/de not_active IP Right Cessation
- 1970-11-16 CS CS74548A patent/CS165317B2/cs unknown
- 1970-11-16 CS CS74547A patent/CS165316B2/cs unknown
- 1970-11-17 SU SU701495559D patent/SU452962A3/ru active
- 1970-11-17 SU SU1495559A patent/SU429583A3/ru active
- 1970-11-23 NL NL7017108A patent/NL7017108A/xx unknown
- 1970-11-26 FR FR7042588A patent/FR2115622A5/fr not_active Expired
- 1970-11-27 BE BE759524D patent/BE759524A/xx unknown
- 1970-12-14 US US00098026A patent/US3794641A/en not_active Expired - Lifetime
-
1975
- 1975-04-17 CH CH1676070A patent/CH583210A5/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| SU437297A3 (ru) | 1974-07-25 |
| GB1324718A (en) | 1973-07-25 |
| CH583210A5 (enExample) | 1976-12-31 |
| CS165317B2 (en) | 1975-12-22 |
| BE759524A (en) | 1971-04-30 |
| CH557828A (de) | 1975-01-15 |
| SU452962A3 (ru) | 1974-12-05 |
| FR2115622A5 (enExample) | 1972-07-07 |
| US3794641A (en) | 1974-02-26 |
| NL7017108A (enExample) | 1972-05-25 |
| CS165316B2 (en) | 1975-12-22 |
| CH564551A5 (enExample) | 1975-07-31 |
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