JPH0466236B2 - - Google Patents
Info
- Publication number
- JPH0466236B2 JPH0466236B2 JP16745084A JP16745084A JPH0466236B2 JP H0466236 B2 JPH0466236 B2 JP H0466236B2 JP 16745084 A JP16745084 A JP 16745084A JP 16745084 A JP16745084 A JP 16745084A JP H0466236 B2 JPH0466236 B2 JP H0466236B2
- Authority
- JP
- Japan
- Prior art keywords
- hydroxyquinoxaline
- halogeno
- reaction
- peroxide
- acid
- 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
- 150000002978 peroxides Chemical class 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 5
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 230000001590 oxidative effect Effects 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 description 13
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000013078 crystal Substances 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- HHLFWLYXYJOTON-UHFFFAOYSA-N glyoxylic acid Chemical compound OC(=O)C=O HHLFWLYXYJOTON-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- SJAZZQLTKBYDHN-UHFFFAOYSA-N 6-chloro-1h-quinoxalin-2-one Chemical compound C1=C(Cl)C=CC2=NC(O)=CN=C21 SJAZZQLTKBYDHN-UHFFFAOYSA-N 0.000 description 3
- HOOMNCITVCXDTR-UHFFFAOYSA-N 6-chloroquinoxaline Chemical compound N1=CC=NC2=CC(Cl)=CC=C21 HOOMNCITVCXDTR-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 3
- 239000012452 mother liquor Substances 0.000 description 3
- DPJCXCZTLWNFOH-UHFFFAOYSA-N 2-nitroaniline Chemical class NC1=CC=CC=C1[N+]([O-])=O DPJCXCZTLWNFOH-UHFFFAOYSA-N 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- 230000002378 acidificating effect Effects 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- WASQWSOJHCZDFK-UHFFFAOYSA-N diketene Chemical compound C=C1CC(=O)O1 WASQWSOJHCZDFK-UHFFFAOYSA-N 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- 230000033444 hydroxylation Effects 0.000 description 2
- 238000005805 hydroxylation reaction Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 150000004987 o-phenylenediamines Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
- RNOLFZACEWWIHP-UHFFFAOYSA-N 6-chloro-1,4-dihydroquinoxaline-2,3-dione Chemical compound N1C(=O)C(=O)NC2=CC(Cl)=CC=C21 RNOLFZACEWWIHP-UHFFFAOYSA-N 0.000 description 1
- DSZWPJSGTPEFJI-UHFFFAOYSA-N 6-chloro-2-methoxyquinoxaline Chemical compound COc1cnc2cc(Cl)ccc2n1 DSZWPJSGTPEFJI-UHFFFAOYSA-N 0.000 description 1
- HIDXVGIAGDJBIN-UHFFFAOYSA-N 7-chloro-1h-quinoxalin-2-one Chemical compound N1=CC(=O)NC2=CC(Cl)=CC=C21 HIDXVGIAGDJBIN-UHFFFAOYSA-N 0.000 description 1
- 150000001204 N-oxides Chemical class 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- DKAGJZJALZXOOV-UHFFFAOYSA-N hydrate;hydrochloride Chemical compound O.Cl DKAGJZJALZXOOV-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- XCRBXWCUXJNEFX-UHFFFAOYSA-N peroxybenzoic acid Chemical class OOC(=O)C1=CC=CC=C1 XCRBXWCUXJNEFX-UHFFFAOYSA-N 0.000 description 1
- FFRYUAVNPBUEIC-UHFFFAOYSA-N quinoxalin-2-ol Chemical compound C1=CC=CC2=NC(O)=CN=C21 FFRYUAVNPBUEIC-UHFFFAOYSA-N 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16745084A JPS6144877A (ja) | 1984-08-10 | 1984-08-10 | 6−ハロゲノ−2−ヒドロキシキノキザリンの製法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16745084A JPS6144877A (ja) | 1984-08-10 | 1984-08-10 | 6−ハロゲノ−2−ヒドロキシキノキザリンの製法 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6144877A JPS6144877A (ja) | 1986-03-04 |
JPH0466236B2 true JPH0466236B2 (enrdf_load_stackoverflow) | 1992-10-22 |
Family
ID=15849918
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16745084A Granted JPS6144877A (ja) | 1984-08-10 | 1984-08-10 | 6−ハロゲノ−2−ヒドロキシキノキザリンの製法 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6144877A (enrdf_load_stackoverflow) |
-
1984
- 1984-08-10 JP JP16745084A patent/JPS6144877A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6144877A (ja) | 1986-03-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE2315801B2 (de) | 2-Alkyl-3-acyl-pyrazolo [1,5-a] pyridine, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneipräparate | |
JP2630134B2 (ja) | テトラヒドロフタルイミド化合物の製造法 | |
JPH0466236B2 (enrdf_load_stackoverflow) | ||
Dime et al. | Synthesis of isoquinolines from indenes | |
CZ339598A3 (cs) | Způsob výroby formylimidazolů | |
US2799676A (en) | ||
JP3010264B2 (ja) | イソクマリン類の製造方法 | |
JP4418104B2 (ja) | ホルミルイミダゾールの製法 | |
JP2950948B2 (ja) | 3―メチルキノリン―8―カルボン酸の製造法 | |
JP3831021B2 (ja) | 2−インダノン類の製造方法 | |
EP0663394B1 (en) | Process for preparing 5-aminodihydropyrrole, intermediate thereof and process for preparing said intermediate | |
US5169955A (en) | Process for producing 2-hydroxyquinoxaline derivatives | |
DE69101937T2 (de) | Antiallergische und antiinflammatorische Mittel auf der Basis von Benzoquinon. | |
WO2005023787A1 (en) | Process for the manufacture of 2,1,3-benzoxadiazole-4-carboxaldehyde | |
KR100194062B1 (ko) | 다양한 치환체를 갖는 2-시클로헥센온의 제조방법 | |
CA2334901C (en) | Procedure for producing formyl imidazoles | |
JP2860676B2 (ja) | 1―イソキノリン類の製造方法 | |
US6469178B2 (en) | Procedure for producing formylimidazoles | |
JPS6119618B2 (enrdf_load_stackoverflow) | ||
JP2907475B2 (ja) | (1,2,3―チアジアゾール―4―イル)カルボアルデヒドの製造方法及び中間体 | |
JPS6326745B2 (enrdf_load_stackoverflow) | ||
JP4066100B2 (ja) | N−アシル含窒素環状ケトン類の製造方法 | |
EP0086438A1 (en) | Process and intermediates for preparing 4-hydroxymethyl-1-phthalazone derivatives | |
JPH0825970B2 (ja) | テトラヒドロフタルイミド系化合物の製造法、その中間体および該中間体の製造法 | |
JP2002348286A (ja) | イミダゾール化合物の製造方法、およびその中間体 |