JPS6338996B2 - - Google Patents
Info
- Publication number
- JPS6338996B2 JPS6338996B2 JP10538980A JP10538980A JPS6338996B2 JP S6338996 B2 JPS6338996 B2 JP S6338996B2 JP 10538980 A JP10538980 A JP 10538980A JP 10538980 A JP10538980 A JP 10538980A JP S6338996 B2 JPS6338996 B2 JP S6338996B2
- Authority
- JP
- Japan
- Prior art keywords
- formula
- sulfur
- general formula
- multiplet
- ethanol
- 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
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 239000011593 sulfur Substances 0.000 claims description 6
- IJAPPYDYQCXOEF-UHFFFAOYSA-N phthalazin-1(2H)-one Chemical class C1=CC=C2C(=O)NN=CC2=C1 IJAPPYDYQCXOEF-UHFFFAOYSA-N 0.000 claims description 5
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- -1 N-cyano-S-methyl-N′-[3-(1- oxo-4-phenyl-2-phthalazinyl) Propyl]isothiourea Chemical compound 0.000 description 2
- 238000000862 absorption spectrum Methods 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000012442 inert solvent Substances 0.000 description 2
- 238000001819 mass spectrum Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 2
- 208000002874 Acne Vulgaris Diseases 0.000 description 1
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 206010020601 Hyperchlorhydria Diseases 0.000 description 1
- 208000008469 Peptic Ulcer Diseases 0.000 description 1
- UHGKYJXJYJWDAM-UHFFFAOYSA-N Propylthiourea Chemical compound CCCNC(N)=S UHGKYJXJYJWDAM-UHFFFAOYSA-N 0.000 description 1
- 241000700159 Rattus Species 0.000 description 1
- 208000007107 Stomach Ulcer Diseases 0.000 description 1
- 208000025865 Ulcer Diseases 0.000 description 1
- 229960001138 acetylsalicylic acid Drugs 0.000 description 1
- 206010000496 acne Diseases 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 208000000718 duodenal ulcer Diseases 0.000 description 1
- 210000004211 gastric acid Anatomy 0.000 description 1
- 210000004051 gastric juice Anatomy 0.000 description 1
- 201000005917 gastric ulcer Diseases 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000028327 secretion Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 1
- 231100000397 ulcer Toxicity 0.000 description 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10538980A JPS5728064A (en) | 1980-07-29 | 1980-07-29 | Phthalazinone derivative |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10538980A JPS5728064A (en) | 1980-07-29 | 1980-07-29 | Phthalazinone derivative |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5728064A JPS5728064A (en) | 1982-02-15 |
JPS6338996B2 true JPS6338996B2 (enrdf_load_stackoverflow) | 1988-08-03 |
Family
ID=14406288
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP10538980A Granted JPS5728064A (en) | 1980-07-29 | 1980-07-29 | Phthalazinone derivative |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5728064A (enrdf_load_stackoverflow) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0309765A3 (en) * | 1987-09-30 | 1990-09-26 | Fisons Corporation | 1(2h)-phthalazinones as cytoprotective agents |
-
1980
- 1980-07-29 JP JP10538980A patent/JPS5728064A/ja active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5728064A (en) | 1982-02-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS635389B2 (enrdf_load_stackoverflow) | ||
DE69128477T2 (de) | Benzopyranderivat | |
DE69626682T2 (de) | Verfahren zur herstellung von guanidinderivaten, zwischenprodukte dafür und ihre herstellung | |
US4526608A (en) | Certain 2-pyridyloxyphenyl-oximino-ether-carboxylates, herbicidal compositions containing same and their herbicidal method of use | |
US3906024A (en) | Perfluoroalkanesulfonamidoaryl compounds | |
US3920690A (en) | Herbicidal trifluoromethylsulfonamido-pyrazoles | |
US3923810A (en) | Perfluoroalkanesulfonamides N-substituted by heterocyclic groups | |
JPS6338996B2 (enrdf_load_stackoverflow) | ||
EP0095104B1 (en) | Process for the preparation of pyridyl and quinolyl imidazolinones | |
EP0057564A1 (en) | Process for preparing 3,5-diamino-1,2,4-triazoles | |
DE10353205A1 (de) | Ortho-substituierte Pentafluorsulfuranyl-Benzole, Verfahren zu ihrer Herstellung sowie ihre Verwendung als wertvolle Synthese-Zwischenstufen | |
US3923811A (en) | Perfluoroalkanesulfonamides N-substituted by heterocyclic groups | |
JPS6325587B2 (enrdf_load_stackoverflow) | ||
US3801588A (en) | Certain perfluoroalkylsulfon-amidothiazoles | |
JPS6242900B2 (enrdf_load_stackoverflow) | ||
US3161680A (en) | Nu-alkyl-nu-benzyl-beta-thiopropionamides | |
JPS6338993B2 (enrdf_load_stackoverflow) | ||
JPS6340189B2 (enrdf_load_stackoverflow) | ||
JPH0143750B2 (enrdf_load_stackoverflow) | ||
JPS6340187B2 (enrdf_load_stackoverflow) | ||
SE441357B (sv) | 4-pyridino - cyanoguanidinderivat, forfarande for framstellning av detta samt en komposition med blodtryckssenkande verkan | |
Galli et al. | 1, 3-Acyl migration in carbonic acid derivatives—synthesis of S-polyhalogenoalkyl N-acyl-N-aryl (alkyl) thiocarbamates | |
AT276437B (de) | Verfahren zur Herstellung von neuen Carbamaten von Pyridinmethanolderivaten | |
US3261861A (en) | N-cyano-glycinonitriles preparatory process | |
AT345832B (de) | Verfahren zur herstellung neuer pyridinderivate und ihrer salze |