JPS6241712B2 - - Google Patents
Info
- Publication number
- JPS6241712B2 JPS6241712B2 JP59190157A JP19015784A JPS6241712B2 JP S6241712 B2 JPS6241712 B2 JP S6241712B2 JP 59190157 A JP59190157 A JP 59190157A JP 19015784 A JP19015784 A JP 19015784A JP S6241712 B2 JPS6241712 B2 JP S6241712B2
- Authority
- JP
- Japan
- Prior art keywords
- dithiazolium
- compounds
- perchlorate
- phenyl
- salt
- 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
- -1 3-aryl-5-disubstituted amino-1,4,2-dithiazolium salt Chemical class 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 150000001450 anions Chemical class 0.000 claims description 2
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 8
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- MNNJLAZJQBWSST-UHFFFAOYSA-N 1,4,2-dithiazole Chemical class C1SC=NS1 MNNJLAZJQBWSST-UHFFFAOYSA-N 0.000 description 5
- 230000009102 absorption Effects 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 238000000921 elemental analysis Methods 0.000 description 4
- 239000000575 pesticide Substances 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 238000000862 absorption spectrum Methods 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 239000003905 agrochemical Substances 0.000 description 2
- XQIJUNRYEIASNK-UHFFFAOYSA-N amino carbamodithioate Chemical class NSC(N)=S XQIJUNRYEIASNK-UHFFFAOYSA-N 0.000 description 2
- BTBUDFIPZVFTDQ-UHFFFAOYSA-N benzamido n,n-diethylcarbamodithioate Chemical compound CCN(CC)C(=S)SNC(=O)C1=CC=CC=C1 BTBUDFIPZVFTDQ-UHFFFAOYSA-N 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- IIGQRYLVHFWKHJ-UHFFFAOYSA-N 1,3-dithiol-1-ium Chemical class C1=C[S+]=CS1 IIGQRYLVHFWKHJ-UHFFFAOYSA-N 0.000 description 1
- XTLFOTGRJYJFTE-UHFFFAOYSA-N 3h-1,2,4-dithiazole Chemical class C1SSC=N1 XTLFOTGRJYJFTE-UHFFFAOYSA-N 0.000 description 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
- 229910020366 ClO 4 Inorganic materials 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001768 cations Chemical group 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- SYBMFSCJUKHJQP-UHFFFAOYSA-N dithiazol-1-ium Chemical class S1[S+]=NC=C1 SYBMFSCJUKHJQP-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000001072 heteroaryl group Chemical group 0.000 description 1
- ZLTPDFXIESTBQG-UHFFFAOYSA-N isothiazole Chemical class C=1C=NSC=1 ZLTPDFXIESTBQG-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0622—Heterocyclic compounds
- G03G5/0624—Heterocyclic compounds containing one hetero ring
- G03G5/0627—Heterocyclic compounds containing one hetero ring being five-membered
- G03G5/0633—Heterocyclic compounds containing one hetero ring being five-membered containing three hetero atoms
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Photoreceptors In Electrophotography (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59190157A JPS6168480A (ja) | 1984-09-11 | 1984-09-11 | ３−アリ−ル−５−ジ置換アミノ−１，４，２−ジチアゾリウム塩 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59190157A JPS6168480A (ja) | 1984-09-11 | 1984-09-11 | ３−アリ−ル−５−ジ置換アミノ−１，４，２−ジチアゾリウム塩 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6168480A JPS6168480A (ja) | 1986-04-08 |
| JPS6241712B2 true JPS6241712B2 (OSRAM) | 1987-09-04 |
Family
ID=16253368
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59190157A Granted JPS6168480A (ja) | 1984-09-11 | 1984-09-11 | ３−アリ−ル−５−ジ置換アミノ−１，４，２−ジチアゾリウム塩 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6168480A (OSRAM) |
-
1984
- 1984-09-11 JP JP59190157A patent/JPS6168480A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6168480A (ja) | 1986-04-08 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Sommer et al. | Alkylation of amines. New method for the synthesis of quaternary ammonium compounds from primary and secondary amines | |
| KR920002295B1 (ko) | 프롤리디논 유도체의 제조방법 | |
| EP0052333B1 (en) | 4-fluoro-5-oxypyrazole derivate and preparation thereof | |
| JPS6241712B2 (OSRAM) | ||
| US2574505A (en) | Process of preparing 2, 2-diphenyl-3-methyl-4-dimethylamino butyronitrile | |
| JPS6241713B2 (OSRAM) | ||
| HU188074B (en) | Process for the preparation of cimetidin | |
| US3226379A (en) | Novel 1,3-bis(polyhydroxyalkyl)-2-imidazolidinones and 1,3-bis(polyhydroxyalkyl)-imidazolidine-2-thiones | |
| US4048211A (en) | Modification of methadone synthesis process step | |
| Smith et al. | Amidrazones 9. Convenient Syntheses of 1-Alkyl-1-Phenylhydrazines and α, β-Unsaturated Amidrazones Via Base-Promoted Reactions of 1, 1-Disubstituted-3-Amino-4, 5-Dihydro-1H-Pyrazolium Salts | |
| KR20030083007A (ko) | 5-치환 옥사졸 화합물 및 5-치환 이미다졸 화합물의제조방법 | |
| US2975186A (en) | Certain haloalkylolamino pyridines | |
| CA1100514A (en) | Imidazolidine derivatives useful as insecticides and acaricides | |
| CN107857729B (zh) | 一种4-碘化-n-芳基化的吡唑类化合物的合成方法 | |
| KR0180562B1 (ko) | 2-메틸-4-이소티아졸린-3-온염 혼합물의 제조방법 | |
| KR800001451B1 (ko) | 1, 3, 5-트리치환 벤젠 유도체의 제법 | |
| Guan et al. | Helical Structures of Tribenzylamine Supramolecular Complexes with [CoCl4] 2−/[CuCl4] 2−, and Conformational Comparisons of Tribenzylamine in Different Supramolecular Complexes | |
| US4960917A (en) | Process for the preparation of an acexamic acid derivatives | |
| JPS6272680A (ja) | ラニチジン又はその酸付加塩の製造方法 | |
| SU481605A1 (ru) | Способ получени производных 1-замещенных диформилдитиопирролдионов | |
| JPS5914465B2 (ja) | ２，４，６−トリ置換−１，３，５−チアジアジニリウム塩の製造法 | |
| CA1226869A (en) | Process for the preparation of enamines; novel enamines and the use of enamines in the preparation of dihydropyridines | |
| JPS5919947B2 (ja) | ２，４，６−トリ置換−１，３，５−チアジアジニリウム塩 | |
| JPS60190760A (ja) | ピロリジン誘導体及びその製造法 | |
| JPS5923314B2 (ja) | 新規ピロ−ル誘導体 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |