JP2010530379A5 - - Google Patents
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- Publication number
- JP2010530379A5 JP2010530379A5 JP2010512548A JP2010512548A JP2010530379A5 JP 2010530379 A5 JP2010530379 A5 JP 2010530379A5 JP 2010512548 A JP2010512548 A JP 2010512548A JP 2010512548 A JP2010512548 A JP 2010512548A JP 2010530379 A5 JP2010530379 A5 JP 2010530379A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- optionally substituted
- cycloalkyl
- group
- carbon atoms
- 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.)
- Abandoned
Links
- 125000004432 carbon atom Chemical group C* 0.000 claims 16
- 238000000034 method Methods 0.000 claims 16
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 11
- 229910052801 chlorine Inorganic materials 0.000 claims 11
- 239000000460 chlorine Substances 0.000 claims 11
- 125000000217 alkyl group Chemical group 0.000 claims 10
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 8
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 8
- 125000003342 alkenyl group Chemical group 0.000 claims 8
- 125000000304 alkynyl group Chemical group 0.000 claims 8
- 125000003118 aryl group Chemical group 0.000 claims 8
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 8
- 229910052794 bromium Inorganic materials 0.000 claims 8
- 150000001875 compounds Chemical class 0.000 claims 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims 8
- 229910052731 fluorine Inorganic materials 0.000 claims 8
- 239000011737 fluorine Substances 0.000 claims 8
- 229910052736 halogen Inorganic materials 0.000 claims 8
- 150000002367 halogens Chemical class 0.000 claims 8
- 125000001424 substituent group Chemical group 0.000 claims 8
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 7
- -1 C 1- C 4 -alkylthio Chemical group 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 125000003545 alkoxy group Chemical group 0.000 claims 4
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 4
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 4
- 125000003282 alkyl amino group Chemical group 0.000 claims 4
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 4
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 4
- 125000004414 alkyl thio group Chemical group 0.000 claims 4
- 125000002947 alkylene group Chemical group 0.000 claims 4
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 4
- 125000001072 heteroaryl group Chemical group 0.000 claims 4
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 125000000858 thiocyanato group Chemical group *SC#N 0.000 claims 4
- 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 claims 3
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 3
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 claims 2
- 238000005660 chlorination reaction Methods 0.000 claims 2
- 238000005580 one pot reaction Methods 0.000 claims 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 claims 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 claims 2
- 125000004665 trialkylsilyl group Chemical group 0.000 claims 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 150000005125 dioxazines Chemical class 0.000 claims 1
- HCUYBXPSSCRKRF-UHFFFAOYSA-N diphosgene Chemical compound ClC(=O)OC(Cl)(Cl)Cl HCUYBXPSSCRKRF-UHFFFAOYSA-N 0.000 claims 1
- 125000004438 haloalkoxy group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 239000011630 iodine Substances 0.000 claims 1
- RLOWWWKZYUNIDI-UHFFFAOYSA-N phosphinic chloride Chemical compound ClP=O RLOWWWKZYUNIDI-UHFFFAOYSA-N 0.000 claims 1
- 238000007363 ring formation reaction Methods 0.000 claims 1
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07011965A EP2009001A1 (de) | 2007-06-19 | 2007-06-19 | Verfahren zur Herstellung von Dioxazin-Derivaten |
| PCT/EP2008/004215 WO2008155004A1 (de) | 2007-06-19 | 2008-05-28 | Verfahren zur herstellung von dioxazin-derivaten |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010530379A JP2010530379A (ja) | 2010-09-09 |
| JP2010530379A5 true JP2010530379A5 (enExample) | 2011-06-16 |
Family
ID=38669355
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010512548A Abandoned JP2010530379A (ja) | 2007-06-19 | 2008-05-28 | ジオキサジン誘導体の製造方法 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20100184973A1 (enExample) |
| EP (2) | EP2009001A1 (enExample) |
| JP (1) | JP2010530379A (enExample) |
| CN (1) | CN101687804A (enExample) |
| BR (1) | BRPI0813255A2 (enExample) |
| IL (1) | IL202756A0 (enExample) |
| MX (1) | MX2009014191A (enExample) |
| TW (1) | TW200916466A (enExample) |
| WO (1) | WO2008155004A1 (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107987068A (zh) * | 2017-12-08 | 2018-05-04 | 青岛清原化合物有限公司 | 一种二噁嗪衍生物及其制备方法、除草组合物和应用 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3420824A (en) * | 1966-07-26 | 1969-01-07 | Du Pont | 5-oxo-1,4,2-dioxazines and preparation from alpha-amidooxy acids |
| DE4336875A1 (de) * | 1993-09-27 | 1995-03-30 | Bayer Ag | N-Azinyl-N'-(het)arylsulfonyl-harnstoffe |
| RU2004107485A (ru) * | 2001-08-15 | 2005-03-27 | Е.И.Дюпон де Немур энд Компани (US) | Орто-гетероциклические замещенные ариламиды для борьбы с беспозвоночными вредителями |
| CN1950368B (zh) * | 2004-04-27 | 2011-08-31 | 日产化学工业株式会社 | 吡唑磺酰脲化合物和除草剂 |
| DE102005033581B4 (de) * | 2005-07-19 | 2007-04-26 | Lanxess Deutschland Gmbh | Organische Pigmente für Farbfilter |
| DE102005044108A1 (de) * | 2005-09-15 | 2007-03-29 | Bayer Cropscience Ag | Dioxazin- und Oxdiazin-substituierte Arylamide |
-
2007
- 2007-06-19 EP EP07011965A patent/EP2009001A1/de not_active Withdrawn
-
2008
- 2008-05-28 EP EP08758800A patent/EP2167467A1/de not_active Withdrawn
- 2008-05-28 WO PCT/EP2008/004215 patent/WO2008155004A1/de not_active Ceased
- 2008-05-28 JP JP2010512548A patent/JP2010530379A/ja not_active Abandoned
- 2008-05-28 CN CN200880020768A patent/CN101687804A/zh active Pending
- 2008-05-28 US US12/664,924 patent/US20100184973A1/en not_active Abandoned
- 2008-05-28 BR BRPI0813255-0A2A patent/BRPI0813255A2/pt not_active IP Right Cessation
- 2008-05-28 MX MX2009014191A patent/MX2009014191A/es unknown
- 2008-06-17 TW TW097122568A patent/TW200916466A/zh unknown
-
2009
- 2009-12-15 IL IL202756A patent/IL202756A0/en unknown