PL56544B1 - - Google Patents
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- Publication number
- PL56544B1 PL56544B1 PL111562A PL11156265A PL56544B1 PL 56544 B1 PL56544 B1 PL 56544B1 PL 111562 A PL111562 A PL 111562A PL 11156265 A PL11156265 A PL 11156265A PL 56544 B1 PL56544 B1 PL 56544B1
- Authority
- PL
- Poland
- Prior art keywords
- ethyl
- physiologically tolerable
- dimethoxybenzyl
- poultry feed
- pyrimidine
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 2
- 244000144977 poultry Species 0.000 claims 2
- NHZLNPMOSADWGC-UHFFFAOYSA-N 4-amino-N-(2-quinoxalinyl)benzenesulfonamide Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=CN=C(C=CC=C2)C2=N1 NHZLNPMOSADWGC-UHFFFAOYSA-N 0.000 claims 1
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical group O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 claims 1
- 239000003674 animal food additive Substances 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 235000015097 nutrients Nutrition 0.000 claims 1
- 150000003230 pyrimidines Chemical class 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 229960003097 sulfaquinoxaline Drugs 0.000 claims 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 4
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ISAKRJDGNUQOIC-UHFFFAOYSA-N Uracil Chemical compound O=C1C=CNC(=O)N1 ISAKRJDGNUQOIC-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- XKXRCHAIPLHHEZ-UHFFFAOYSA-N 5-[(2-ethyl-4,5-dimethoxyphenyl)methyl]-1H-pyrimidine-2,4-dione Chemical compound C(C)C1=C(CC=2C(NC(NC2)=O)=O)C=C(C(=C1)OC)OC XKXRCHAIPLHHEZ-UHFFFAOYSA-N 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- CBHOOMGKXCMKIR-UHFFFAOYSA-N azane;methanol Chemical compound N.OC CBHOOMGKXCMKIR-UHFFFAOYSA-N 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229940035893 uracil Drugs 0.000 description 1
Description
Otrzymany roztwór wlano do roztworu 40 g 30 jodku sodowego w 300 ml 3 N wodnego roztworu wodorotlenku sodowego. Nitrobenzen kilkakrot¬ nie ekstrahowano benzenem, a wodny roztwór ekstrahowano kwasem octowym, przy czym otrzy¬ mano 25 g 5-(2,-etylo-4,) 5'-dwumetoksybenzylo) 35 uracylu o temperaturze topnienia 219 do 220°. 21 g 5-(2'-etylo-4', 5'-dwumetoksybenzylo)uracy- lu, 84 ml tlenochlorku fosforu i 1,5 ml dwume- tyloaniliny ogrzewano w ciagu 4-ch godzin pod chlodnica zwrotna podczas mieszania. Nadmiar 40 tlenochlorku fosforu oddestylowano pod próznia, a syropowata pozostalosc rozkladano za pomoca lodowatej wody. Otrzymana 2,4-dwuchloro-5-(2'- -etylo-4\ 5,-dwumetoksy-benzylo)pirymidyne eks¬ trahowano octanem etylu i wyodrebniono ja w 45 postaci krystalicznej pozostalosci (20 g) o tempe¬ raturze topnienia 71 do 72° (z metanolu) po od¬ parowaniu rozpuszczalnika. 20 g. ^-dwuchloro-S-^-etylo-^, 5'-dwumeto- ksy-benzylo) pirymidyny ogrzewano w ciagu 6 go- 50 dzin przy temperaturze 140 do 160°, w autokla¬ wie z 300 ml metanolowego amoniaku, wysycone- go przy temperaturze 0°. Po ochlodzeniu miesza¬ niny reakcyjnej krystalizowala czesciowo 2,4-2 amilno-5-(2,-etylo-4,, 5'-dwumetoksybenzylo) piiry- midyne. Reszte tego zwiazku otrzymano po odpa¬ rowaniu lugu macierzystego. Po przekrystalizowa- niu 60% etanolu otrzymano 2,4-2 amino-5-<2,-etylo- -4', 5'-dwumetoksybenzylo) pirymidyne o tempe¬ raturze topnienia 206—207° w postaci bezbarwnych cn krysztalów. bU PL
Claims (1)
1. Zastrzezenie, patentowe Sposób wytwarzania paszy dla drobiu lub do¬ datku do pasz dla drobiu, znamienny tym, ze 65 sulfadimetoksyne, sulfachinoksaline lub sulfameto-56544 ksazol oraz nowa pochodna pirymidynowa o ogól¬ nym wzorze 1, w którym R oznacza grupe meto- ksylowa, metylowa lub etylowa, albo fizjologicz- 8 nie znoszona sól tego zwiazku miesza sie z subs¬ tancjami zywieniowymi lub substancjami fizjolo¬ gicznie znoszonymi. OCH, oca Lub. Zakl. Graf. Zam. 3136. 30.IX.68. 220 PL
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL56544B1 true PL56544B1 (pl) | 1968-10-25 |
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