SE190894C1 - - Google Patents
Info
- Publication number
- SE190894C1 SE190894C1 SE190894DA SE190894C1 SE 190894 C1 SE190894 C1 SE 190894C1 SE 190894D A SE190894D A SE 190894DA SE 190894 C1 SE190894 C1 SE 190894C1
- Authority
- SE
- Sweden
- Prior art keywords
- chlorine
- oxidizing agent
- oxazine
- hydantoin
- pyrido
- Prior art date
Links
- 229910052801 chlorine Inorganic materials 0.000 claims description 11
- 239000000460 chlorine Substances 0.000 claims description 11
- 239000007800 oxidant agent Substances 0.000 claims description 8
- 229940091173 hydantoin Drugs 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 3
- PAOWOJRQGBFDQG-UHFFFAOYSA-N pyrido[2,3-e][1,3]oxazine-2,4-dione Chemical compound C1=CC=C2OC(=O)NC(=O)C2=N1 PAOWOJRQGBFDQG-UHFFFAOYSA-N 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 229960000583 acetic acid Drugs 0.000 description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- HORQAOAYAYGIBM-UHFFFAOYSA-N 2,4-dinitrophenylhydrazine Chemical compound NNC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O HORQAOAYAYGIBM-UHFFFAOYSA-N 0.000 description 1
- DXMYTBSZYATUTO-UHFFFAOYSA-N 2H-1,3-oxazine hydrochloride Chemical compound Cl.O1CN=CC=C1 DXMYTBSZYATUTO-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- GEFUOUGNUMYCBB-UHFFFAOYSA-N Cl.O=C1OC2=C(C(N1)=O)N=CC=C2 Chemical compound Cl.O=C1OC2=C(C(N1)=O)N=CC=C2 GEFUOUGNUMYCBB-UHFFFAOYSA-N 0.000 description 1
- 239000005708 Sodium hypochlorite Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- FBAFATDZDUQKNH-UHFFFAOYSA-M iron chloride Chemical compound [Cl-].[Fe] FBAFATDZDUQKNH-UHFFFAOYSA-M 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000004893 oxazines Chemical class 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SE190894T |
Publications (1)
Publication Number | Publication Date |
---|---|
SE190894C1 true SE190894C1 (enrdf_load_stackoverflow) | 1964-01-01 |
Family
ID=41977461
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SE190894D SE190894C1 (enrdf_load_stackoverflow) |
Country Status (1)
Country | Link |
---|---|
SE (1) | SE190894C1 (enrdf_load_stackoverflow) |
-
0
- SE SE190894D patent/SE190894C1/sv unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103601680A (zh) | 双吡唑环类含能化合物及其制备方法 | |
JPH0329791B2 (enrdf_load_stackoverflow) | ||
CN114105984A (zh) | 吲哚嗪类抗蚀剂的制备方法 | |
US2027030A (en) | Thiazoline compound | |
SE190894C1 (enrdf_load_stackoverflow) | ||
US2952677A (en) | Aminoguanadine compounds | |
PL94736B1 (pl) | Sposob wytwarzania 2-triazolo(3,4-b)-benzotiazoli | |
US2073600A (en) | Heterocyclic hydrazines | |
JPS626590B2 (enrdf_load_stackoverflow) | ||
US3474135A (en) | N-(omega-aminoalkylene)-aminoalkyl sulfonic acids | |
US3410852A (en) | Process for preparing 3, 4-dihydro-2, 4-dioxo-2h-pyrido[2, 3-e][1, 3]oxazine | |
BRPI0516994B1 (pt) | Processo para preparação de pirazóis, uso e processo para a alquilação regiosseletiva | |
US2410619A (en) | Sulfamyl benzotriazoles | |
US1765678A (en) | Process for introducing sulphocyanic groups into organic compounds | |
Kobelevskaya et al. | Sulfonation of unsymmetrically substituted 5-chloropyrazoles. | |
US2019529A (en) | Aminobenzothiazole compound | |
US2216515A (en) | Production of nitro-mercaptodiphenylamines | |
US2430051A (en) | Soluble sulfanilamide derivatives and process of preparing them | |
US1016784A (en) | Organic mercury compound. | |
US2184491A (en) | Process for the production of polyhydroxy-fuchsone derivatives by means of aliphaticgroups | |
US1867105A (en) | New process for preparing p-nitroso-amine compounds of the aromatic series and the compounds obtainable thereby | |
US4185020A (en) | 5-(4-Nitrophenyl)-2-furanmethanamines derivatives | |
US1081079A (en) | Art of making derivatives of dinitro-methylnitramino-phenyl-arsinic acids. | |
US2072238A (en) | Manufacture of naphthalene derivatives | |
US3117121A (en) | Phenoxathinyl glyoxal derivatives |