HU180289B - Process for producing s-triasihe derivatives - Google Patents
Process for producing s-triasihe derivatives Download PDFInfo
- Publication number
- HU180289B HU180289B HU79RO1042A HURO001042A HU180289B HU 180289 B HU180289 B HU 180289B HU 79RO1042 A HU79RO1042 A HU 79RO1042A HU RO001042 A HURO001042 A HU RO001042A HU 180289 B HU180289 B HU 180289B
- Authority
- HU
- Hungary
- Prior art keywords
- formula
- urea
- preparation
- amidino
- methyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 59
- 230000008569 process Effects 0.000 title claims description 36
- SQSPRWMERUQXNE-UHFFFAOYSA-N Guanylurea Chemical compound NC(=N)NC(N)=O SQSPRWMERUQXNE-UHFFFAOYSA-N 0.000 claims abstract description 18
- JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical class C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 claims abstract description 7
- 150000001875 compounds Chemical class 0.000 claims description 84
- 238000002360 preparation method Methods 0.000 claims description 38
- -1 hydrogen ions Chemical class 0.000 claims description 22
- 125000000217 alkyl group Chemical group 0.000 claims description 19
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- 150000003839 salts Chemical class 0.000 claims description 13
- 238000007363 ring formation reaction Methods 0.000 claims description 12
- 239000001257 hydrogen Substances 0.000 claims description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- 229910052736 halogen Inorganic materials 0.000 claims description 10
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- 229910052757 nitrogen Inorganic materials 0.000 claims description 9
- ZSXGLVDWWRXATF-UHFFFAOYSA-N N,N-dimethylformamide dimethyl acetal Chemical compound COC(OC)N(C)C ZSXGLVDWWRXATF-UHFFFAOYSA-N 0.000 claims description 7
- 229910052760 oxygen Inorganic materials 0.000 claims description 7
- 239000008194 pharmaceutical composition Substances 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 6
- 231100000252 nontoxic Toxicity 0.000 claims description 6
- 230000003000 nontoxic effect Effects 0.000 claims description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
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- 229910052717 sulfur Chemical group 0.000 claims description 5
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- FBZVZUSVGKOWHG-UHFFFAOYSA-N 1,1-dimethoxy-n,n-dimethylethanamine Chemical group COC(C)(OC)N(C)C FBZVZUSVGKOWHG-UHFFFAOYSA-N 0.000 claims description 2
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- CVXYGLCPHOOIIL-UHFFFAOYSA-N 3-(diaminomethylidene)-1-(2,6-dimethylphenyl)-1-methylurea Chemical compound NC(N)=NC(=O)N(C)C1=C(C)C=CC=C1C CVXYGLCPHOOIIL-UHFFFAOYSA-N 0.000 claims 1
- PNNCWTXUWKENPE-UHFFFAOYSA-N [N].NC(N)=O Chemical compound [N].NC(N)=O PNNCWTXUWKENPE-UHFFFAOYSA-N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
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- 150000001408 amides Chemical class 0.000 abstract description 9
- OPOJRMTZHYUKLY-UHFFFAOYSA-N 1h-1,3,5-triazin-2-one Chemical class O=C1N=CN=CN1 OPOJRMTZHYUKLY-UHFFFAOYSA-N 0.000 abstract description 7
- 230000000144 pharmacologic effect Effects 0.000 abstract description 7
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- OKGXJRGLYVRVNE-UHFFFAOYSA-N diaminomethylidenethiourea Chemical class NC(N)=NC(N)=S OKGXJRGLYVRVNE-UHFFFAOYSA-N 0.000 abstract description 4
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- 239000000725 suspension Substances 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 5
- 239000003708 ampul Substances 0.000 description 5
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- 239000003610 charcoal Substances 0.000 description 5
- 239000000460 chlorine Substances 0.000 description 5
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 5
- 229940079593 drug Drugs 0.000 description 5
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- 239000000523 sample Substances 0.000 description 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 4
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/14—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom
- C07D251/16—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hydrogen or carbon atoms directly attached to at least one ring carbon atom to only one ring carbon atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/10—Laxatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/12—Antidiarrhoeals
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/959,611 US4246409A (en) | 1978-11-13 | 1978-11-13 | Triazinones |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HU180289B true HU180289B (en) | 1983-02-28 |
Family
ID=25502213
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU79RO1042A HU180289B (en) | 1978-11-13 | 1979-11-13 | Process for producing s-triasihe derivatives |
Country Status (17)
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4452980A (en) * | 1981-01-15 | 1984-06-05 | William H. Rorer, Inc. | Triazinones |
| US4387225A (en) * | 1981-01-15 | 1983-06-07 | William H. Rorer, Inc. | Heterocyclic alkylene triazinones |
| US4443456A (en) * | 1981-05-12 | 1984-04-17 | William H. Rorer, Inc. | Pyridyl alkylene amidinoureas |
| USRE33125E (en) * | 1981-07-06 | 1989-12-05 | Rorer Pharmaceutical Corporation | 3- and 5-[3-(1-arylureido)]-1,2,4-triazoles |
| US4406897A (en) * | 1981-07-06 | 1983-09-27 | William H. Rorer, Inc. | 6-Aryl-4-hydrazinyl-s-triazin-2-ones |
| US4460585A (en) * | 1981-07-06 | 1984-07-17 | William H. Rorer, Inc. | 1-Aryl-4-hydrazinyl-s-triazin-2-ones |
| EP0073276A1 (en) * | 1981-08-24 | 1983-03-09 | Rorer International (Overseas) Inc. | A method of increasing the feed efficiency of animals, and compositions for use in such a method |
| US4562188A (en) * | 1984-01-13 | 1985-12-31 | William H. Rorer, Inc. | Triazinones for treating irritable bowel syndrome |
| WO2011109383A1 (en) * | 2010-03-02 | 2011-09-09 | Southern Research Institute | Use of 2'-deoxy -4'-thiocytidine and its analogues as dna hypomethylating anticancer agents |
| JPWO2015050212A1 (ja) * | 2013-10-02 | 2017-03-09 | 日産化学工業株式会社 | Ｔ型カルシウムチャネル阻害剤 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1287910A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1968-12-19 | 1972-09-06 | ||
| IL42103A (en) * | 1972-05-24 | 1976-05-31 | Du Pont | 6-amino-s-triazine-2,4-(1h,3h)-diones and corresponding 4-thio compounds,their preparation and their use as herbicides |
| US4068081A (en) * | 1974-02-15 | 1978-01-10 | Imperial Chemical Industries Limited | Δ-Triazine-2,6-dione |
-
1978
- 1978-11-13 US US05/959,611 patent/US4246409A/en not_active Expired - Lifetime
-
1979
- 1979-11-07 CA CA000339405A patent/CA1136136A/en not_active Expired
- 1979-11-12 PH PH23273A patent/PH17430A/en unknown
- 1979-11-12 AU AU52735/79A patent/AU530790B2/en not_active Ceased
- 1979-11-12 ZA ZA00796079A patent/ZA796079B/xx unknown
- 1979-11-13 CH CH10138/79A patent/CH647515A5/de not_active IP Right Cessation
- 1979-11-13 DE DE19792945701 patent/DE2945701A1/de not_active Ceased
- 1979-11-13 MX MX798483U patent/MX6832E/es unknown
- 1979-11-13 FR FR7927874A patent/FR2441617A1/fr active Granted
- 1979-11-13 IT IT27243/79A patent/IT1193334B/it active
- 1979-11-13 JP JP14697079A patent/JPS5572174A/ja active Granted
- 1979-11-13 HU HU79RO1042A patent/HU180289B/hu unknown
- 1979-11-13 ES ES485929A patent/ES485929A0/es active Granted
- 1979-11-13 NL NL7908287A patent/NL7908287A/nl not_active Application Discontinuation
- 1979-11-13 BE BE0/198083A patent/BE879990A/fr not_active IP Right Cessation
- 1979-11-13 GB GB7939190A patent/GB2039891B/en not_active Expired
- 1979-11-18 AR AR278877A patent/AR226547A1/es active
Also Published As
| Publication number | Publication date |
|---|---|
| IT7927243A0 (it) | 1979-11-13 |
| AU530790B2 (en) | 1983-07-28 |
| ES8100278A1 (es) | 1980-11-01 |
| AR226547A1 (es) | 1982-07-30 |
| US4246409A (en) | 1981-01-20 |
| FR2441617B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1983-08-26 |
| ZA796079B (en) | 1980-12-31 |
| ES485929A0 (es) | 1980-11-01 |
| CH647515A5 (de) | 1985-01-31 |
| BE879990A (fr) | 1980-05-13 |
| GB2039891A (en) | 1980-08-20 |
| CA1136136A (en) | 1982-11-23 |
| JPS6365664B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1988-12-16 |
| FR2441617A1 (fr) | 1980-06-13 |
| IT1193334B (it) | 1988-06-15 |
| GB2039891B (en) | 1983-05-05 |
| JPS5572174A (en) | 1980-05-30 |
| PH17430A (en) | 1984-08-20 |
| MX6832E (es) | 1986-08-15 |
| AU5273579A (en) | 1980-05-22 |
| NL7908287A (nl) | 1980-05-16 |
| DE2945701A1 (de) | 1980-08-07 |
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