SE122866C1 - - Google Patents
Info
- Publication number
- SE122866C1 SE122866C1 SE122866DA SE122866C1 SE 122866 C1 SE122866 C1 SE 122866C1 SE 122866D A SE122866D A SE 122866DA SE 122866 C1 SE122866 C1 SE 122866C1
- Authority
- SE
- Sweden
- Prior art keywords
- formaldehyde
- sulfanilamido
- parts
- preparation
- pyrimidine
- Prior art date
Links
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 33
- 239000007859 condensation product Substances 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 3
- 150000007513 acids Chemical class 0.000 claims description 3
- ASWVTGNCAZCNNR-UHFFFAOYSA-N sulfamethazine Chemical compound CC1=CC(C)=NC(NS(=O)(=O)C=2C=CC(N)=CC=2)=N1 ASWVTGNCAZCNNR-UHFFFAOYSA-N 0.000 claims description 2
- QPPBRPIAZZHUNT-UHFFFAOYSA-N sulfamerazine Chemical compound CC1=CC=NC(NS(=O)(=O)C=2C=CC(N)=CC=2)=N1 QPPBRPIAZZHUNT-UHFFFAOYSA-N 0.000 claims 2
- SEEPANYCNGTZFQ-UHFFFAOYSA-N sulfadiazine Chemical compound C1=CC(N)=CC=C1S(=O)(=O)NC1=NC=CC=N1 SEEPANYCNGTZFQ-UHFFFAOYSA-N 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 239000008098 formaldehyde solution Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- VKYKSIONXSXAKP-UHFFFAOYSA-N hexamethylenetetramine Chemical compound C1N(C2)CN3CN1CN2C3 VKYKSIONXSXAKP-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- 241000283725 Bos Species 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000004312 hexamethylene tetramine Substances 0.000 description 1
- 235000010299 hexamethylene tetramine Nutrition 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE122866T |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SE122866C1 true SE122866C1 (enExample) | 1948-01-01 |
Family
ID=41922024
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE122866D SE122866C1 (enExample) |
Country Status (1)
| Country | Link |
|---|---|
| SE (1) | SE122866C1 (enExample) |
-
0
- SE SE122866D patent/SE122866C1/sv unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP5247728B2 (ja) | ベンズイミダゾール誘導体の製造方法 | |
| HUE031893T2 (en) | Process for the preparation of 2-ethoxy-1- (2 '- ((hydroxyamino) iminomethyl) biphenyl-4-yl) methyl) -1H-benzo (d) imidazole-7-carboxylic acid and its esters | |
| SE122866C1 (enExample) | ||
| RU2019140915A (ru) | Полилизиновое производное и его применение в композициях на основе твердого вещества | |
| US3321464A (en) | 3-carbo hydrocarbonoxy amino crotonamides and process for the preparation of uracils therefrom | |
| US2538557A (en) | Sulfanilamidopyrimidine-formaldehyde condensation products | |
| Yale | The skraup reaction with acrolein and its derivatives. I. The preparation of 6-Methoxy-8-nitroquinoline | |
| SE122867C1 (enExample) | ||
| CN109867709B (zh) | 具有抗肿瘤作用的甘草次酸系列衍生物(toga-x)的制备方法和应用 | |
| IL44341A (en) | 6-substituted 3-carbethoxyhydrazinopyridazines their preparation and pharmaceutical compositions containing them | |
| US2544660A (en) | Benzeydrylurea addition compound and method for preparing same | |
| SE127567C1 (enExample) | ||
| US2671788A (en) | New pyrimidine derivatives | |
| SE122328C1 (enExample) | ||
| US20250051255A1 (en) | Method for synthesizing tyloxapol | |
| US3280119A (en) | Sulfonamide compound of benzothiadiazine series and process for preparing the same | |
| CN107162989A (zh) | 一种甲氧苄啶杂质的制备方法 | |
| JP2018509467A (ja) | 1,2,5−チアジアゾリジン−1,1−ジオキシドの塩形態、結晶形態及びその調製方法と中間体 | |
| SU70499A1 (ru) | Способ получени сульфанилилгуанидина | |
| CN104803981A (zh) | 一种哌啶-4-胺基二芳基嘧啶衍生物及其制备方法和用途 | |
| GB790203A (en) | Improvements in and relating to naphthalene derivatives and the manufacture thereof | |
| SU393280A1 (ru) | Способ получения 3-(\'-алкил-или n^n'-диaлkилamиhoaцetил)- | |
| SE124739C1 (enExample) | ||
| SE174574C1 (enExample) | ||
| Simonoff | New Compounds. p-Benzyloxy-α-methylbenzyl Alcohol |