IL93730A - History of triphenyl phosphonium-H-1 thiano-) D-3,4 (- imidazole-H3) - Google Patents
History of triphenyl phosphonium-H-1 thiano-) D-3,4 (- imidazole-H3)Info
- Publication number
- IL93730A IL93730A IL9373090A IL9373090A IL93730A IL 93730 A IL93730 A IL 93730A IL 9373090 A IL9373090 A IL 9373090A IL 9373090 A IL9373090 A IL 9373090A IL 93730 A IL93730 A IL 93730A
- Authority
- IL
- Israel
- Prior art keywords
- group
- thieno
- imidazol
- formula
- substituted
- Prior art date
Links
- 239000000543 intermediate Substances 0.000 title abstract description 6
- FOIMGWXSRXJOEX-UHFFFAOYSA-N 2-(2-oxo-3,3a,6,6a-tetrahydro-1H-thieno[3,4-d]imidazol-4-ylidene)pentanoic acid Chemical class N1C(NC2C1CSC2=C(C(=O)O)CCC)=O FOIMGWXSRXJOEX-UHFFFAOYSA-N 0.000 title abstract description 3
- CEQQLHQBLQGVHX-UHFFFAOYSA-N O=C1NC2=CSC=C2N1.C(C=C1)=CC=C1P(C1=CC=CC=C1)C1=CC=CC=C1 Chemical class O=C1NC2=CSC=C2N1.C(C=C1)=CC=C1P(C1=CC=CC=C1)C1=CC=CC=C1 CEQQLHQBLQGVHX-UHFFFAOYSA-N 0.000 title description 2
- 238000000034 method Methods 0.000 claims abstract description 18
- -1 phosphonium compound Chemical class 0.000 claims description 27
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 9
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 239000012442 inert solvent Substances 0.000 claims description 6
- 150000004714 phosphonium salts Chemical class 0.000 claims description 6
- 239000003638 chemical reducing agent Substances 0.000 claims description 5
- SIPUZPBQZHNSDW-UHFFFAOYSA-N diisobutylaluminium hydride Substances CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 claims description 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 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 5
- 229910052783 alkali metal Inorganic materials 0.000 claims description 4
- 239000007795 chemical reaction product Substances 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 150000002440 hydroxy compounds Chemical class 0.000 claims description 3
- 150000002969 pentanoic acid esters Chemical class 0.000 claims description 3
- AVNVFKLQLHPRDZ-UHFFFAOYSA-N 3,3a,6,6a-tetrahydro-1h-thieno[3,4-d]imidazole-2,4-dione Chemical class C1SC(=O)C2NC(=O)NC21 AVNVFKLQLHPRDZ-UHFFFAOYSA-N 0.000 claims description 2
- 125000002252 acyl group Chemical group 0.000 claims description 2
- 229910000102 alkali metal hydride Inorganic materials 0.000 claims description 2
- 150000008046 alkali metal hydrides Chemical class 0.000 claims description 2
- 150000001340 alkali metals Chemical group 0.000 claims description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims description 2
- 125000005160 aryl oxy alkyl group Chemical group 0.000 claims description 2
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 claims description 2
- MOOAHMCRPCTRLV-UHFFFAOYSA-N boron sodium Chemical compound [B].[Na] MOOAHMCRPCTRLV-UHFFFAOYSA-N 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 claims description 2
- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 claims description 2
- 125000004665 trialkylsilyl group Chemical group 0.000 claims description 2
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 claims 2
- 101100490437 Mus musculus Acvrl1 gene Proteins 0.000 claims 1
- 229910000091 aluminium hydride Inorganic materials 0.000 claims 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 1
- 229910000085 borane Inorganic materials 0.000 claims 1
- YBJHBAHKTGYVGT-ZKWXMUAHSA-N (+)-Biotin Chemical compound N1C(=O)N[C@@H]2[C@H](CCCCC(=O)O)SC[C@@H]21 YBJHBAHKTGYVGT-ZKWXMUAHSA-N 0.000 abstract description 15
- 238000002360 preparation method Methods 0.000 abstract description 8
- 239000013543 active substance Substances 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 21
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 15
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- 239000011541 reaction mixture Substances 0.000 description 7
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- BMTAFVWTTFSTOG-UHFFFAOYSA-N Butylate Chemical compound CCSC(=O)N(CC(C)C)CC(C)C BMTAFVWTTFSTOG-UHFFFAOYSA-N 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229960002685 biotin Drugs 0.000 description 3
- 235000020958 biotin Nutrition 0.000 description 3
- 239000011616 biotin Substances 0.000 description 3
- 239000003480 eluent Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000010898 silica gel chromatography Methods 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- RJTYEFFUXNIXHA-MGONOCMRSA-N CCCC(=C1[C@@H]2[C@H](CS1)N(C(=O)N2CC3=CC=CC=C3)[C@H](C)C4=CC=CC=C4)C(=O)OCC5=CC=CC=C5 Chemical compound CCCC(=C1[C@@H]2[C@H](CS1)N(C(=O)N2CC3=CC=CC=C3)[C@H](C)C4=CC=CC=C4)C(=O)OCC5=CC=CC=C5 RJTYEFFUXNIXHA-MGONOCMRSA-N 0.000 description 2
- RMHXJMOESAJCNJ-UIUQJESISA-N CCCCCCOC(=O)C(=C1[C@@H]2[C@H](CS1)N(C(=O)N2CC3=CC=CC=C3)[C@H](C)C4=CC=CC=C4)CCC Chemical compound CCCCCCOC(=O)C(=C1[C@@H]2[C@H](CS1)N(C(=O)N2CC3=CC=CC=C3)[C@H](C)C4=CC=CC=C4)CCC RMHXJMOESAJCNJ-UIUQJESISA-N 0.000 description 2
- FKLJPTJMIBLJAV-UHFFFAOYSA-N Compound IV Chemical compound O1N=C(C)C=C1CCCCCCCOC1=CC=C(C=2OCCN=2)C=C1 FKLJPTJMIBLJAV-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 238000003747 Grignard reaction Methods 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 238000007239 Wittig reaction Methods 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000002045 lasting effect Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- WRIKHQLVHPKCJU-UHFFFAOYSA-N sodium bis(trimethylsilyl)amide Chemical compound C[Si](C)(C)N([Na])[Si](C)(C)C WRIKHQLVHPKCJU-UHFFFAOYSA-N 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 2
- NBYZKUYZEJXDQM-QPZJVUEUSA-N (3ar,6as)-1-benzyl-6-hydroxy-3-[(1r)-1-phenylethyl]-3a,4,6,6a-tetrahydrothieno[3,4-d]imidazol-2-one Chemical compound N1([C@@H]2C(O)SC[C@@H]2N(C1=O)[C@H](C)C=1C=CC=CC=1)CC1=CC=CC=C1 NBYZKUYZEJXDQM-QPZJVUEUSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- 125000004217 4-methoxybenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C([H])([H])* 0.000 description 1
- VBKPPDYGFUZOAJ-UHFFFAOYSA-N 5-oxopentanoic acid Chemical compound OC(=O)CCCC=O VBKPPDYGFUZOAJ-UHFFFAOYSA-N 0.000 description 1
- 206010048768 Dermatosis Diseases 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 229930003756 Vitamin B7 Natural products 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 235000019270 ammonium chloride Nutrition 0.000 description 1
- LOGJGIGNTMIGTB-UHFFFAOYSA-N benzyl 5-oxopentanoate Chemical compound O=CCCCC(=O)OCC1=CC=CC=C1 LOGJGIGNTMIGTB-UHFFFAOYSA-N 0.000 description 1
- UORVGPXVDQYIDP-BJUDXGSMSA-N borane Chemical class [10BH3] UORVGPXVDQYIDP-BJUDXGSMSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000002778 food additive Substances 0.000 description 1
- 235000013373 food additive Nutrition 0.000 description 1
- ZREIXECYDRCUTO-UHFFFAOYSA-N hexyl 5-oxopentanoate Chemical compound CCCCCCOC(=O)CCCC=O ZREIXECYDRCUTO-UHFFFAOYSA-N 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
- YBTZROCKNUIONO-UHFFFAOYSA-N methyl 5-oxopentanoate Chemical compound COC(=O)CCCC=O YBTZROCKNUIONO-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- HNBDRPTVWVGKBR-UHFFFAOYSA-N methyl pentanoate Chemical compound CCCCC(=O)OC HNBDRPTVWVGKBR-UHFFFAOYSA-N 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 208000017520 skin disease Diseases 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- AVCVDUDESCZFHJ-UHFFFAOYSA-N triphenylphosphane;hydrochloride Chemical compound [Cl-].C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1 AVCVDUDESCZFHJ-UHFFFAOYSA-N 0.000 description 1
- RIOQSEWOXXDEQQ-UHFFFAOYSA-O triphenylphosphanium Chemical compound C1=CC=CC=C1[PH+](C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-O 0.000 description 1
- 229940005605 valeric acid Drugs 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011735 vitamin B7 Substances 0.000 description 1
- 235000011912 vitamin B7 Nutrition 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6561—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH95389 | 1989-03-15 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL93730A0 IL93730A0 (en) | 1990-12-23 |
| IL93730A true IL93730A (en) | 1996-01-19 |
Family
ID=4199016
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL9373090A IL93730A (en) | 1989-03-15 | 1990-03-13 | History of triphenyl phosphonium-H-1 thiano-) D-3,4 (- imidazole-H3) |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US5084578A (no) |
| EP (1) | EP0387747B1 (no) |
| JP (1) | JPH02282388A (no) |
| AT (1) | ATE122676T1 (no) |
| CA (1) | CA2011793A1 (no) |
| DD (1) | DD292460A5 (no) |
| DE (1) | DE59009076D1 (no) |
| DK (1) | DK0387747T3 (no) |
| ES (1) | ES2072326T3 (no) |
| FI (1) | FI95034C (no) |
| GE (1) | GEP19970939B (no) |
| HU (1) | HU203892B (no) |
| IE (1) | IE67771B1 (no) |
| IL (1) | IL93730A (no) |
| LT (1) | LT3192B (no) |
| NO (1) | NO174151C (no) |
| PT (1) | PT93437B (no) |
| RU (1) | RU1838314C (no) |
| YU (1) | YU45190A (no) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5252743A (en) * | 1989-11-13 | 1993-10-12 | Affymax Technologies N.V. | Spatially-addressable immobilization of anti-ligands on surfaces |
| CN109503620B (zh) * | 2018-12-25 | 2020-10-16 | 浙江新和成股份有限公司 | 5-(2-氧代四氢噻吩并咪唑-4(2h)-烯基)戊酸类化合物的制备方法 |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2784191A (en) * | 1957-03-05 | Process for the production of lactams | ||
| US2489232A (en) * | 1949-11-22 | Synthesis of biotin | ||
| US2489235A (en) * | 1947-07-24 | 1949-11-22 | Hoffmann La Roche | Synthesis of biotin |
| US2535010A (en) * | 1948-10-02 | 1950-12-19 | Rohm & Haas | Transetherification of beta-ethersubstituted esters |
| DE850007C (de) * | 1950-12-22 | 1952-09-22 | Basf Ag | Verfahren zur Herstellung von N-Aryl-ª‡-pyrrolidonen |
| BE759512A (fr) * | 1969-11-29 | 1971-05-27 | Hoffmann La Roche | Lactone |
| US4054740A (en) * | 1974-12-24 | 1977-10-18 | Hoffmann-La Roche Inc. | Hydroxybiotin |
| IT1045043B (it) * | 1975-08-13 | 1980-04-21 | Isf Spa | Derivati pirrolidinici |
| JPS6050455B2 (ja) * | 1976-07-16 | 1985-11-08 | オリンパス光学工業株式会社 | 内視鏡 |
| JPS5315074A (en) * | 1976-07-28 | 1978-02-10 | Nippon Telegr & Teleph Corp <Ntt> | Mask alignment method |
| IT1075564B (it) * | 1977-02-11 | 1985-04-22 | Isf Spa | Procedimento per la preparazione di derivati pirrolidinici |
| IT1075280B (it) * | 1977-02-11 | 1985-04-22 | Isf Spa | Procedimento per la preparazione di derivati pirrolidinici |
| DE3018109A1 (de) * | 1980-05-12 | 1981-11-19 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von biotin sowie neue ausgangsverbindungen fuer dieses verfahren |
| JPS5812272B2 (ja) * | 1981-04-28 | 1983-03-07 | 電気化学工業株式会社 | ４−ヒドロキシ−２−ピロリドンの製造法 |
| JPS58124791A (ja) * | 1982-01-19 | 1983-07-25 | Sumitomo Chem Co Ltd | ビオチンの製造法 |
| DE3580390D1 (de) * | 1984-05-18 | 1990-12-13 | Hoffmann La Roche | Verfahren zur herstellung eines lactons. |
| DE3575717D1 (de) * | 1984-08-25 | 1990-03-08 | Merck Patent Gmbh | Verfahren zur herstellung von (3a5,6ar)-und/oder(3ar,6a5)-1,3-dibenzyl-hexahydro-1h-furo(3,4-d)imidazol-2,4-dion. |
| DE3505652A1 (de) * | 1985-02-19 | 1986-08-21 | I.G. Bauerhin GmbH elektro-technische Fabrik, 6466 Gründau | Verfahren zum elektrischen beheizen von insbesondere fahrzeugsitzen |
| FI83510C (fi) * | 1985-02-22 | 1991-07-25 | Ciba Geigy Ag | Foerfarande foer framstaellning av nya, terapeutiskt anvaendbara bi-2h- pyrroli(di)ndioner. |
| CH670644A5 (no) * | 1986-12-18 | 1989-06-30 | Lonza Ag | |
| CH671227A5 (no) * | 1986-12-02 | 1989-08-15 | Lonza Ag | |
| US5236252A (en) * | 1991-12-18 | 1993-08-17 | Alliedsignal Inc. | Method of skid dection without speed sensors |
-
1990
- 1990-02-16 FI FI900787A patent/FI95034C/fi not_active IP Right Cessation
- 1990-03-06 YU YU00451/90A patent/YU45190A/xx unknown
- 1990-03-08 CA CA002011793A patent/CA2011793A1/en not_active Abandoned
- 1990-03-08 IE IE83690A patent/IE67771B1/en not_active IP Right Cessation
- 1990-03-09 JP JP2059786A patent/JPH02282388A/ja active Pending
- 1990-03-09 DD DD90338550A patent/DD292460A5/de not_active IP Right Cessation
- 1990-03-12 DE DE59009076T patent/DE59009076D1/de not_active Expired - Fee Related
- 1990-03-12 EP EP90104620A patent/EP0387747B1/de not_active Expired - Lifetime
- 1990-03-12 AT AT90104620T patent/ATE122676T1/de active
- 1990-03-12 ES ES90104620T patent/ES2072326T3/es not_active Expired - Lifetime
- 1990-03-12 DK DK90104620.1T patent/DK0387747T3/da not_active Application Discontinuation
- 1990-03-12 US US07/491,589 patent/US5084578A/en not_active Expired - Fee Related
- 1990-03-13 IL IL9373090A patent/IL93730A/en not_active IP Right Cessation
- 1990-03-14 RU SU904743316A patent/RU1838314C/ru active
- 1990-03-14 PT PT93437A patent/PT93437B/pt not_active IP Right Cessation
- 1990-03-14 HU HU901581A patent/HU203892B/hu not_active IP Right Cessation
- 1990-03-14 NO NO901190A patent/NO174151C/no unknown
- 1990-07-23 US US07/556,187 patent/US5086185A/en not_active Expired - Fee Related
-
1993
- 1993-02-26 LT LTIP359A patent/LT3192B/lt not_active IP Right Cessation
- 1993-07-12 GE GEAP19931002A patent/GEP19970939B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| YU45190A (en) | 1991-10-31 |
| DD292460A5 (de) | 1991-08-01 |
| EP0387747B1 (de) | 1995-05-17 |
| US5086185A (en) | 1992-02-04 |
| FI900787A0 (fi) | 1990-02-16 |
| HU203892B (en) | 1991-10-28 |
| CA2011793A1 (en) | 1990-09-15 |
| LT3192B (en) | 1995-03-27 |
| FI95034B (fi) | 1995-08-31 |
| US5084578A (en) | 1992-01-28 |
| PT93437A (pt) | 1990-11-07 |
| GEP19970939B (en) | 1997-03-26 |
| DE59009076D1 (de) | 1995-06-22 |
| PT93437B (pt) | 1996-08-30 |
| ATE122676T1 (de) | 1995-06-15 |
| RU1838314C (ru) | 1993-08-30 |
| EP0387747A1 (de) | 1990-09-19 |
| NO901190D0 (no) | 1990-03-14 |
| IL93730A0 (en) | 1990-12-23 |
| HU901581D0 (en) | 1990-06-28 |
| IE900836L (en) | 1990-09-15 |
| NO174151B (no) | 1993-12-13 |
| JPH02282388A (ja) | 1990-11-19 |
| IE67771B1 (en) | 1996-04-17 |
| LTIP359A (en) | 1994-09-25 |
| NO174151C (no) | 1994-03-23 |
| DK0387747T3 (da) | 1995-06-06 |
| ES2072326T3 (es) | 1995-07-16 |
| NO901190L (no) | 1990-09-17 |
| FI95034C (fi) | 1995-12-11 |
| HUT55398A (en) | 1991-05-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FF | Patent granted | ||
| KB | Patent renewed | ||
| RH | Patent void |