JPS58164567A - 異項環チオ−ル化合物とその製法 - Google Patents
異項環チオ−ル化合物とその製法Info
- Publication number
- JPS58164567A JPS58164567A JP57047846A JP4784682A JPS58164567A JP S58164567 A JPS58164567 A JP S58164567A JP 57047846 A JP57047846 A JP 57047846A JP 4784682 A JP4784682 A JP 4784682A JP S58164567 A JPS58164567 A JP S58164567A
- Authority
- JP
- Japan
- Prior art keywords
- hydroxyethyl
- ether
- tetrazolethiol
- water
- dithiocarbamate
- 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.)
- Granted
Links
- -1 Heterocyclic thiol compound Chemical class 0.000 title claims description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims abstract description 15
- 150000001875 compounds Chemical class 0.000 claims abstract description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 8
- 150000002170 ethers Chemical class 0.000 claims abstract description 6
- 150000002148 esters Chemical class 0.000 claims abstract description 5
- 239000002994 raw material Substances 0.000 claims abstract description 5
- JUINSXZKUKVTMD-UHFFFAOYSA-N hydrogen azide Chemical compound N=[N+]=[N-] JUINSXZKUKVTMD-UHFFFAOYSA-N 0.000 claims abstract description 3
- 150000003839 salts Chemical class 0.000 claims abstract description 3
- 239000012990 dithiocarbamate Substances 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 6
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 125000006239 protecting group Chemical group 0.000 abstract description 5
- 239000002798 polar solvent Substances 0.000 abstract description 3
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 abstract description 2
- 229930186147 Cephalosporin Natural products 0.000 abstract description 2
- 239000003905 agrochemical Substances 0.000 abstract description 2
- 125000003118 aryl group Chemical group 0.000 abstract description 2
- 229940124587 cephalosporin Drugs 0.000 abstract description 2
- 150000001780 cephalosporins Chemical class 0.000 abstract description 2
- LXUBLWNPXHMMGB-UHFFFAOYSA-N methyl n-(2-trityloxyethyl)carbamodithioate Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(OCCNC(=S)SC)C1=CC=CC=C1 LXUBLWNPXHMMGB-UHFFFAOYSA-N 0.000 abstract description 2
- 150000003536 tetrazoles Chemical group 0.000 abstract description 2
- YKYUEQRWYGVUKB-UHFFFAOYSA-N 1-(2-hydroxyethyl)-2h-tetrazole-5-thione Chemical compound OCCN1N=NN=C1S YKYUEQRWYGVUKB-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 230000003115 biocidal effect Effects 0.000 abstract 1
- 125000001181 organosilyl group Chemical group [SiH3]* 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 33
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- 238000006243 chemical reaction Methods 0.000 description 20
- 239000000203 mixture Substances 0.000 description 16
- 238000003756 stirring Methods 0.000 description 13
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
- 239000000243 solution Substances 0.000 description 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 239000010410 layer Substances 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 5
- GJUIUIJPXQCMFE-UHFFFAOYSA-N methyl n-(2-hydroxyethyl)carbamodithioate Chemical compound CSC(=S)NCCO GJUIUIJPXQCMFE-UHFFFAOYSA-N 0.000 description 5
- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 4
- PLMHQXSIADFDIE-UHFFFAOYSA-N methyl carbamodithioate Chemical compound CSC(N)=S PLMHQXSIADFDIE-UHFFFAOYSA-N 0.000 description 4
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 238000010511 deprotection reaction Methods 0.000 description 2
- 239000012442 inert solvent Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical group CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 description 1
- DIGCWYGXBRVXIW-UHFFFAOYSA-N 1-sulfanyltetrazole Chemical compound SN1C=NN=N1 DIGCWYGXBRVXIW-UHFFFAOYSA-N 0.000 description 1
- JAAIPIWKKXCNOC-UHFFFAOYSA-N 1h-tetrazol-1-ium-5-thiolate Chemical class SC1=NN=NN1 JAAIPIWKKXCNOC-UHFFFAOYSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- NPOMSUOUAZCMBL-UHFFFAOYSA-N dichloromethane;ethoxyethane Chemical compound ClCCl.CCOCC NPOMSUOUAZCMBL-UHFFFAOYSA-N 0.000 description 1
- SPWVRYZQLGQKGK-UHFFFAOYSA-N dichloromethane;hexane Chemical compound ClCCl.CCCCCC SPWVRYZQLGQKGK-UHFFFAOYSA-N 0.000 description 1
- POCFBDFTJMJWLG-UHFFFAOYSA-N dihydrosinapic acid methyl ester Natural products COC(=O)CCC1=CC(OC)=C(O)C(OC)=C1 POCFBDFTJMJWLG-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical group CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- ZKQFHRVKCYFVCN-UHFFFAOYSA-N ethoxyethane;hexane Chemical compound CCOCC.CCCCCC ZKQFHRVKCYFVCN-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 125000004404 heteroalkyl group Chemical group 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000004434 industrial solvent Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000006798 ring closing metathesis reaction Methods 0.000 description 1
- 238000005185 salting out Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- XHFLOLLMZOTPSM-UHFFFAOYSA-M sodium;hydrogen carbonate;hydrate Chemical compound [OH-].[Na+].OC(O)=O XHFLOLLMZOTPSM-UHFFFAOYSA-M 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- JBWKIWSBJXDJDT-UHFFFAOYSA-N triphenylmethyl chloride Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 JBWKIWSBJXDJDT-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (14)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57047846A JPS58164567A (ja) | 1982-03-24 | 1982-03-24 | 異項環チオ−ル化合物とその製法 |
| US06/475,410 US4508909A (en) | 1982-03-24 | 1983-03-15 | Synthesis of hydroxyethyltetrazolethiol and etherified intermediates therefor |
| SE8301440A SE454174B (sv) | 1982-03-24 | 1983-03-16 | Forfarande for framstellning av 1-hydroxietyl-1h-tetrazol-5-tiol |
| DE3310174A DE3310174C2 (de) | 1982-03-24 | 1983-03-21 | Verfahren zur Herstellung von Hydroxyäthyltetrazolthiol |
| HU83978A HU189674B (en) | 1982-03-24 | 1983-03-23 | Improved process for preparing hydroxyethyl-tetrazole-thiol |
| IT67324/83A IT1162844B (it) | 1982-03-24 | 1983-03-23 | Procedimento per la sintesi di 1idrossietil 1h tetrazol 5 tiolo e dei suoi sali mercapturi |
| FR8304761A FR2523969B1 (fr) | 1982-03-24 | 1983-03-23 | Procede de synthese d'hydroxyethyltetrazolethiols et nouveaux esters alkyliques d'acides n-(hydroxy protege ethyl)dithiocarbamiques et composes de 1-(hydroxy protege ethyl)-1h-tetrazole-5-thiol |
| NLAANVRAGE8301039,A NL189710C (nl) | 1982-03-24 | 1983-03-23 | Werkwijze ter bereiding van hydroxyethyltetrazoolthiol. |
| KR1019830001159A KR880001997B1 (ko) | 1982-03-24 | 1983-03-23 | 히드록시에틸테트라졸티올의 개량 합성방법 |
| ES520879A ES8404996A1 (es) | 1982-03-24 | 1983-03-23 | Un procedimiento para preparar 1-hidroxietil-1h-tetrazol-5-tiolopcionalmente protegido. |
| CH1633/83A CH658054A5 (de) | 1982-03-24 | 1983-03-24 | Tetrazolverbindungen und verfahren zu ihrer herstellung. |
| GB08308127A GB2117767B (en) | 1982-03-24 | 1983-03-24 | Synthesis of hydroxyethyltetrazolethiol |
| CA000424337A CA1192205A (en) | 1982-03-24 | 1983-03-24 | Synthesis of hydroxyethyltetrazolethiol |
| FR8314107A FR2530240B1 (fr) | 1982-03-24 | 1983-09-02 | Nouveaux esters alkyliques d'acides n-(hydroxy protege ethyl) dithiocarbamiques |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57047846A JPS58164567A (ja) | 1982-03-24 | 1982-03-24 | 異項環チオ−ル化合物とその製法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS58164567A true JPS58164567A (ja) | 1983-09-29 |
| JPH0347269B2 JPH0347269B2 (en, 2012) | 1991-07-18 |
Family
ID=12786726
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57047846A Granted JPS58164567A (ja) | 1982-03-24 | 1982-03-24 | 異項環チオ−ル化合物とその製法 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4508909A (en, 2012) |
| JP (1) | JPS58164567A (en, 2012) |
| KR (1) | KR880001997B1 (en, 2012) |
| CA (1) | CA1192205A (en, 2012) |
| CH (1) | CH658054A5 (en, 2012) |
| DE (1) | DE3310174C2 (en, 2012) |
| ES (1) | ES8404996A1 (en, 2012) |
| FR (2) | FR2523969B1 (en, 2012) |
| GB (1) | GB2117767B (en, 2012) |
| HU (1) | HU189674B (en, 2012) |
| IT (1) | IT1162844B (en, 2012) |
| NL (1) | NL189710C (en, 2012) |
| SE (1) | SE454174B (en, 2012) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004168775A (ja) * | 2002-11-08 | 2004-06-17 | Orchid Chemicals & Pharmaceuticals Ltd | オキサセファロスポリンの改良合成法 |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102875484A (zh) * | 2012-09-18 | 2013-01-16 | 江西金顿生物科技有限公司 | 一种1-羟乙基-5-巯基-1h-四氮唑的制备方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3778508A (en) * | 1969-11-07 | 1973-12-11 | Monsanto Co | Feed compositions and methods |
| JPS5082067A (en, 2012) * | 1973-10-31 | 1975-07-03 | ||
| JPS5168568A (en) * | 1974-12-09 | 1976-06-14 | Fujisawa Pharmaceutical Co | 11 chikan 1hh tetorazooru 55 chiooruruino seizoho |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL7414119A (nl) * | 1973-10-31 | 1975-05-02 | Fujisawa Pharmaceutical Co | Werkwijze ter bereiding van 1h-tetrazool-5-thiol- derivaten en 1-gesubstitueerde 1h-tetrazool- -5-thiolen. |
| JPS5168588A (en) * | 1974-12-09 | 1976-06-14 | Meiji Seika Co | Sefuemujudotaino shinkiseizohoho |
| BE845338A (fr) * | 1975-09-02 | 1977-02-21 | Nouvelles cephalosporines, procede pour leur obtention et application pharmaceutique | |
| US5233692A (en) * | 1990-04-06 | 1993-08-03 | Micro Technology, Inc. | Enhanced interface permitting multiple-byte parallel transfers of control information and data on a small computer system interface (SCSI) communication bus and a mass storage system incorporating the enhanced interface |
-
1982
- 1982-03-24 JP JP57047846A patent/JPS58164567A/ja active Granted
-
1983
- 1983-03-15 US US06/475,410 patent/US4508909A/en not_active Expired - Lifetime
- 1983-03-16 SE SE8301440A patent/SE454174B/sv not_active IP Right Cessation
- 1983-03-21 DE DE3310174A patent/DE3310174C2/de not_active Expired - Lifetime
- 1983-03-23 ES ES520879A patent/ES8404996A1/es not_active Expired
- 1983-03-23 IT IT67324/83A patent/IT1162844B/it active
- 1983-03-23 HU HU83978A patent/HU189674B/hu unknown
- 1983-03-23 FR FR8304761A patent/FR2523969B1/fr not_active Expired
- 1983-03-23 NL NLAANVRAGE8301039,A patent/NL189710C/xx active Search and Examination
- 1983-03-23 KR KR1019830001159A patent/KR880001997B1/ko not_active Expired
- 1983-03-24 CA CA000424337A patent/CA1192205A/en not_active Expired
- 1983-03-24 CH CH1633/83A patent/CH658054A5/de not_active IP Right Cessation
- 1983-03-24 GB GB08308127A patent/GB2117767B/en not_active Expired
- 1983-09-02 FR FR8314107A patent/FR2530240B1/fr not_active Expired
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3778508A (en) * | 1969-11-07 | 1973-12-11 | Monsanto Co | Feed compositions and methods |
| JPS5082067A (en, 2012) * | 1973-10-31 | 1975-07-03 | ||
| JPS5168568A (en) * | 1974-12-09 | 1976-06-14 | Fujisawa Pharmaceutical Co | 11 chikan 1hh tetorazooru 55 chiooruruino seizoho |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004168775A (ja) * | 2002-11-08 | 2004-06-17 | Orchid Chemicals & Pharmaceuticals Ltd | オキサセファロスポリンの改良合成法 |
Also Published As
| Publication number | Publication date |
|---|---|
| CA1192205A (en) | 1985-08-20 |
| FR2530240A1 (fr) | 1984-01-20 |
| GB8308127D0 (en) | 1983-05-05 |
| NL8301039A (nl) | 1983-10-17 |
| DE3310174A1 (de) | 1983-09-29 |
| KR880001997B1 (ko) | 1988-10-11 |
| JPH0347269B2 (en, 2012) | 1991-07-18 |
| IT1162844B (it) | 1987-04-01 |
| FR2523969A1 (fr) | 1983-09-30 |
| SE8301440D0 (sv) | 1983-03-16 |
| SE454174B (sv) | 1988-04-11 |
| NL189710B (nl) | 1993-02-01 |
| ES520879A0 (es) | 1984-05-16 |
| GB2117767B (en) | 1985-07-24 |
| FR2530240B1 (fr) | 1986-04-18 |
| SE8301440L (sv) | 1983-09-25 |
| FR2523969B1 (fr) | 1986-02-28 |
| GB2117767A (en) | 1983-10-19 |
| HU189674B (en) | 1986-07-28 |
| IT8367324A0 (it) | 1983-03-23 |
| US4508909A (en) | 1985-04-02 |
| NL189710C (nl) | 1993-07-01 |
| KR840004088A (ko) | 1984-10-06 |
| DE3310174C2 (de) | 1997-02-06 |
| CH658054A5 (de) | 1986-10-15 |
| ES8404996A1 (es) | 1984-05-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SK15892000A3 (sk) | Spôsob syntézy cox-2 inhibítorov a medziprodukty | |
| EP3715342B1 (en) | Fluorosulfonyl-containing compound, intermediate thereof, preparation method therefor and use thereof | |
| WO2013127028A1 (zh) | 一种1-取代-4-溴-1h-1，2，3-三氮唑-5-羧酸的制备方法 | |
| BR112019027323A2 (pt) | método para preparar intermediário de derivado de 4-metoxipirrol | |
| WO2006006290A1 (ja) | １－オキサセファロスポリン－７α－メトキシ－３－クロルメチル誘導体の製法 | |
| Huang et al. | Transition-metal-free and redox-neutral strategy for sulfilimines synthesis via S-arylation of sulfenamides | |
| US20180186753A1 (en) | Processes for the preparation of pesticidal compounds | |
| Tribak et al. | Synthesis and reactivity of new heterocyclic systems derived from 5-chloro-1H-indole-2, 3-dione | |
| JPS58164567A (ja) | 異項環チオ−ル化合物とその製法 | |
| SU622399A3 (ru) | Способ получени солей арилсульфониламидоалкиламинов | |
| AU2004266151B2 (en) | Inhibitors of cathepsin S | |
| Curphey et al. | New synthesis of azaserine | |
| JPS596308B2 (ja) | テトラゾ−ルチオ−ル誘導体 | |
| US2746968A (en) | Novel diacylated hydrazines and process for the manufacture thereof | |
| JPS63316743A (ja) | 脱アシル化方法 | |
| CN110498762A (zh) | 一种(2s,5r)-5-[(苄氧基)氨基]-哌啶-2-甲酸乙酯的合成方法 | |
| JP6887022B2 (ja) | ケトライド化合物を製造するための方法 | |
| US2766257A (en) | Di(omega-carboxyalkyl)-tetrathiocyclodecane | |
| JPS6168455A (ja) | アミド化合物 | |
| SU503517A3 (ru) | Способ получени производных индолилуксусной кислоты или их солей | |
| JPS58198473A (ja) | ヒドロキサム酸誘導体 | |
| JP4913589B2 (ja) | １，２−ベンズイソキサゾール−３−メタンスルホンアミドのワンポット製造法 | |
| JPS58140065A (ja) | メルカプトベンジル脂肪酸誘導体類及びその製法 | |
| Wang et al. | An efficient synthesis of α, β-unsaturated thiol esters | |
| JPS63316755A (ja) | Ｎ−メチル−α−ジアルキルアミノアセトヒドロキサム酸誘導体 |