IL26619A - 2,4-dioxodecahydro-quinazoline compounds substituted in the 1-and 3-position - Google Patents
2,4-dioxodecahydro-quinazoline compounds substituted in the 1-and 3-positionInfo
- Publication number
- IL26619A IL26619A IL26619A IL2661966A IL26619A IL 26619 A IL26619 A IL 26619A IL 26619 A IL26619 A IL 26619A IL 2661966 A IL2661966 A IL 2661966A IL 26619 A IL26619 A IL 26619A
- Authority
- IL
- Israel
- Prior art keywords
- dioxodecahydroquinazoline
- isopropyl
- formula
- compounds
- examples
- Prior art date
Links
- RHSYECGMHASHCW-UHFFFAOYSA-N 4a,5,6,7,8,8a-hexahydro-1h-quinazoline-2,4-dione Chemical group C1CCCC2C(=O)NC(=O)NC21 RHSYECGMHASHCW-UHFFFAOYSA-N 0.000 title claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 24
- 239000004480 active ingredient Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 6
- 125000001589 carboacyl group Chemical group 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000000203 mixture Substances 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 3
- 230000008635 plant growth Effects 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- 230000002363 herbicidal effect Effects 0.000 claims description 2
- 239000012948 isocyanate Substances 0.000 claims description 2
- 150000002513 isocyanates Chemical class 0.000 claims description 2
- 125000005359 phenoxyalkyl group Chemical group 0.000 claims description 2
- 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000004965 chloroalkyl group Chemical group 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 231100000208 phytotoxic Toxicity 0.000 claims 1
- 230000000885 phytotoxic effect Effects 0.000 claims 1
- 239000002689 soil Substances 0.000 claims 1
- 244000024671 Brassica kaber Species 0.000 description 9
- 235000011292 Brassica rapa Nutrition 0.000 description 7
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 7
- 244000292693 Poa annua Species 0.000 description 7
- 241001621841 Alopecurus myosuroides Species 0.000 description 6
- 240000004153 Hibiscus sabdariffa Species 0.000 description 6
- 235000001018 Hibiscus sabdariffa Nutrition 0.000 description 6
- 235000005291 Rumex acetosa Nutrition 0.000 description 6
- 230000006378 damage Effects 0.000 description 6
- 235000003513 sheep sorrel Nutrition 0.000 description 6
- 240000006122 Chenopodium album Species 0.000 description 5
- 235000011498 Chenopodium album var missouriense Nutrition 0.000 description 5
- 235000013328 Chenopodium album var. album Nutrition 0.000 description 5
- 235000014052 Chenopodium album var. microphyllum Nutrition 0.000 description 5
- 235000014050 Chenopodium album var. stevensii Nutrition 0.000 description 5
- 235000013012 Chenopodium album var. striatum Nutrition 0.000 description 5
- 240000003173 Drymaria cordata Species 0.000 description 5
- 240000008042 Zea mays Species 0.000 description 5
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 241000196324 Embryophyta Species 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- HZNXIPDYYIWDNM-UHFFFAOYSA-N 1,2,3,4,4a,5,6,7,8,8a-decahydroquinazoline Chemical compound N1CNCC2CCCCC21 HZNXIPDYYIWDNM-UHFFFAOYSA-N 0.000 description 2
- 235000014750 Brassica kaber Nutrition 0.000 description 2
- 244000025254 Cannabis sativa Species 0.000 description 2
- 240000004585 Dactylis glomerata Species 0.000 description 2
- 244000058871 Echinochloa crus-galli Species 0.000 description 2
- 241001518935 Eragrostis Species 0.000 description 2
- 240000005702 Galium aparine Species 0.000 description 2
- 235000014820 Galium aparine Nutrition 0.000 description 2
- 240000005979 Hordeum vulgare Species 0.000 description 2
- 235000007340 Hordeum vulgare Nutrition 0.000 description 2
- 241000226265 Phanopyrum Species 0.000 description 2
- AEKNYBWUEYNWMJ-QWOOXDRHSA-N Pramiconazole Chemical compound O=C1N(C(C)C)CCN1C1=CC=C(N2CCN(CC2)C=2C=CC(OC[C@@H]3O[C@](CN4N=CN=C4)(CO3)C=3C(=CC(F)=CC=3)F)=CC=2)C=C1 AEKNYBWUEYNWMJ-QWOOXDRHSA-N 0.000 description 2
- 244000061456 Solanum tuberosum Species 0.000 description 2
- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- 244000098338 Triticum aestivum Species 0.000 description 2
- 244000274883 Urtica dioica Species 0.000 description 2
- 235000009108 Urtica dioica Nutrition 0.000 description 2
- 241001148683 Zostera marina Species 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- NZNMSOFKMUBTKW-UHFFFAOYSA-N cyclohexanecarboxylic acid Chemical compound OC(=O)C1CCCCC1 NZNMSOFKMUBTKW-UHFFFAOYSA-N 0.000 description 2
- 230000012010 growth Effects 0.000 description 2
- 239000004009 herbicide Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 235000012015 potatoes Nutrition 0.000 description 2
- GSLTVFIVJMCNBH-UHFFFAOYSA-N 2-isocyanatopropane Chemical compound CC(C)N=C=O GSLTVFIVJMCNBH-UHFFFAOYSA-N 0.000 description 1
- 235000006760 Acer pensylvanicum Nutrition 0.000 description 1
- 241001260012 Bursa Species 0.000 description 1
- 241000219312 Chenopodium Species 0.000 description 1
- FKLJPTJMIBLJAV-UHFFFAOYSA-N Compound IV Chemical compound O1N=C(C)C=C1CCCCCCCOC1=CC=C(C=2OCCN=2)C=C1 FKLJPTJMIBLJAV-UHFFFAOYSA-N 0.000 description 1
- 241000288105 Grus Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000010933 acylation Effects 0.000 description 1
- 238000005917 acylation reaction Methods 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001339 alkali metal compounds Chemical class 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000031018 biological processes and functions Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- DVECBJCOGJRVPX-UHFFFAOYSA-N butyryl chloride Chemical compound CCCC(Cl)=O DVECBJCOGJRVPX-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 244000038559 crop plants Species 0.000 description 1
- VZFUCHSFHOYXIS-UHFFFAOYSA-N cycloheptane carboxylic acid Natural products OC(=O)C1CCCCCC1 VZFUCHSFHOYXIS-UHFFFAOYSA-N 0.000 description 1
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000009331 sowing Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/95—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in positions 2 and 4
- C07D239/96—Two oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEB0084324 | 1965-10-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IL26619A true IL26619A (en) | 1971-04-28 |
Family
ID=6982381
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL26619A IL26619A (en) | 1965-10-30 | 1966-10-03 | 2,4-dioxodecahydro-quinazoline compounds substituted in the 1-and 3-position |
Country Status (10)
| Country | Link |
|---|---|
| AT (1) | AT267251B (enrdf_load_html_response) |
| BE (1) | BE688789A (enrdf_load_html_response) |
| BR (1) | BR6683945D0 (enrdf_load_html_response) |
| CH (1) | CH481574A (enrdf_load_html_response) |
| DE (1) | DE1745901A1 (enrdf_load_html_response) |
| DK (1) | DK115803B (enrdf_load_html_response) |
| ES (1) | ES332903A1 (enrdf_load_html_response) |
| GB (1) | GB1159543A (enrdf_load_html_response) |
| IL (1) | IL26619A (enrdf_load_html_response) |
| NL (1) | NL6615301A (enrdf_load_html_response) |
-
1965
- 1965-10-30 DE DE19651745901 patent/DE1745901A1/de active Pending
-
1966
- 1966-10-03 IL IL26619A patent/IL26619A/en unknown
- 1966-10-12 CH CH1471866A patent/CH481574A/de not_active IP Right Cessation
- 1966-10-24 BR BR183945/66A patent/BR6683945D0/pt unknown
- 1966-10-24 BE BE688789D patent/BE688789A/xx unknown
- 1966-10-28 AT AT1004966A patent/AT267251B/de active
- 1966-10-28 NL NL6615301A patent/NL6615301A/xx unknown
- 1966-10-28 GB GB48420/66A patent/GB1159543A/en not_active Expired
- 1966-10-28 DK DK561466AA patent/DK115803B/da unknown
- 1966-10-29 ES ES0332903A patent/ES332903A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| ES332903A1 (es) | 1967-11-16 |
| NL6615301A (enrdf_load_html_response) | 1967-05-02 |
| CH481574A (de) | 1969-11-30 |
| AT267251B (de) | 1968-12-27 |
| BE688789A (enrdf_load_html_response) | 1967-04-24 |
| GB1159543A (en) | 1969-07-30 |
| DE1745901A1 (de) | 1969-10-16 |
| BR6683945D0 (pt) | 1973-12-04 |
| DK115803B (da) | 1969-11-10 |
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