YU46635B - Postupak za dobijanje tetrazolovih intermedijera - Google Patents
Postupak za dobijanje tetrazolovih intermedijeraInfo
- Publication number
- YU46635B YU46635B YU145189A YU145189A YU46635B YU 46635 B YU46635 B YU 46635B YU 145189 A YU145189 A YU 145189A YU 145189 A YU145189 A YU 145189A YU 46635 B YU46635 B YU 46635B
- Authority
- YU
- Yugoslavia
- Prior art keywords
- formula
- solvent
- reaction
- acid
- group
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 2
- 150000003536 tetrazoles Chemical class 0.000 title abstract 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 abstract 6
- 239000002904 solvent Substances 0.000 abstract 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract 4
- 238000006243 chemical reaction Methods 0.000 abstract 4
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 3
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 238000010992 reflux Methods 0.000 abstract 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- UCMIRNVEIXFBKS-UHFFFAOYSA-N beta-alanine Chemical compound NCCC(O)=O UCMIRNVEIXFBKS-UHFFFAOYSA-N 0.000 abstract 2
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical group O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 abstract 2
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 abstract 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract 2
- MLIREBYILWEBDM-UHFFFAOYSA-M 2-cyanoacetate Chemical compound [O-]C(=O)CC#N MLIREBYILWEBDM-UHFFFAOYSA-M 0.000 abstract 1
- 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 abstract 1
- JWIPGAFCGUDKEY-UHFFFAOYSA-L O[Cr](Cl)(=O)=O.C1=CC=NC=C1 Chemical compound O[Cr](Cl)(=O)=O.C1=CC=NC=C1 JWIPGAFCGUDKEY-UHFFFAOYSA-L 0.000 abstract 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 abstract 1
- 229910052786 argon Inorganic materials 0.000 abstract 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 abstract 1
- 239000012965 benzophenone Substances 0.000 abstract 1
- 229940000635 beta-alanine Drugs 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 abstract 1
- 239000012280 lithium aluminium hydride Substances 0.000 abstract 1
- -1 lithium aluminum hydride Chemical compound 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 238000007127 saponification reaction Methods 0.000 abstract 1
- 238000000926 separation method Methods 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 239000012312 sodium hydride Substances 0.000 abstract 1
- 229910000104 sodium hydride Inorganic materials 0.000 abstract 1
- 125000000335 thiazolyl group Chemical group 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| YU145189A YU46635B (sh) | 1987-02-25 | 1989-07-19 | Postupak za dobijanje tetrazolovih intermedijera |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1855887A | 1987-02-25 | 1987-02-25 | |
| YU36488A YU46781B (sh) | 1987-02-25 | 1988-02-25 | Postupak za dobijanje tetrazolovih intermedijera |
| YU145189A YU46635B (sh) | 1987-02-25 | 1989-07-19 | Postupak za dobijanje tetrazolovih intermedijera |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| YU145189A YU145189A (en) | 1990-04-30 |
| YU46635B true YU46635B (sh) | 1994-01-20 |
Family
ID=21788566
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| YU145189A YU46635B (sh) | 1987-02-25 | 1989-07-19 | Postupak za dobijanje tetrazolovih intermedijera |
Country Status (6)
| Country | Link |
|---|---|
| CN (1) | CN1022564C (cs) |
| CS (1) | CS274669B2 (cs) |
| DD (1) | DD297818A5 (cs) |
| EG (1) | EG18311A (cs) |
| YU (1) | YU46635B (cs) |
| ZA (1) | ZA881278B (cs) |
-
1988
- 1988-02-24 CS CS118188A patent/CS274669B2/cs not_active IP Right Cessation
- 1988-02-24 EG EG10688A patent/EG18311A/xx active
- 1988-02-24 ZA ZA881278A patent/ZA881278B/xx unknown
- 1988-02-25 DD DD31319388A patent/DD297818A5/de unknown
- 1988-02-25 CN CN 88100993 patent/CN1022564C/zh not_active Expired - Fee Related
-
1989
- 1989-07-19 YU YU145189A patent/YU46635B/sh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN1022564C (zh) | 1993-10-27 |
| ZA881278B (en) | 1988-08-25 |
| CS274669B2 (en) | 1991-09-15 |
| CN88100993A (zh) | 1988-09-07 |
| YU145189A (en) | 1990-04-30 |
| CS118188A2 (en) | 1990-11-14 |
| DD297818A5 (de) | 1992-01-23 |
| EG18311A (en) | 1992-10-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2814556A1 (de) | Substituierte phenylessigsaeurederivate und verfahren zu deren herstellung | |
| EP0738703A3 (en) | Acrylic acid derivatives, method for preparing the acrylic acid derivatives, and acrylic acid polymers | |
| JPS5762259A (en) | Preparation of substituted quinolinecarboxylic acid derivative | |
| GB2070609A (en) | Intermediates for the production of picropodophyllin and related compounds | |
| YU46635B (sh) | Postupak za dobijanje tetrazolovih intermedijera | |
| Grieco et al. | Facile retro Diels–Alder reaction of a pentamethyltricyclo [5.2. 1.02, 6] decenone derivative: synthesis of (+)-15 (S)-prostaglandin A2 | |
| YU46781B (sh) | Postupak za dobijanje tetrazolovih intermedijera | |
| JPS62201842A (ja) | ３−ヒドロキシシクロペント−４−エン−１−オン類の製造法 | |
| JPS6032625B2 (ja) | β−チアプロスタン酸系化合物 | |
| JPS54144348A (en) | Preparation of ketone derivative | |
| JPS5721341A (en) | Preparation of substituted acetic ester | |
| JPS57134428A (en) | Production of alpha or beta-irone or its intermediate | |
| US3102133A (en) | 1-[5-(6-methoxy-2-naphthyl)-2-oxycyclopentyl]-2-propanone derivatives | |
| US4238413A (en) | (3-Trifluoromethyl)-benzoyl cyanide and process for its production | |
| ES484576A1 (es) | Procedimiento para la obtencion de esteres de fenoxibencilo del acido bromoestirilciclopropancarboxilico sustituidos,de efecto insecticida y acaricida | |
| US3716558A (en) | 5-propargyl thenyl alcohols | |
| GB2060630A (en) | Pyrazinoquinoline derivatives | |
| JPS5798243A (en) | Preparation of 5-(n-methylaminoethoxy)carvacrol | |
| JPS56108743A (en) | 3-nitro-2-hydroxy-4-phenylbutyric acid derivative, its ester and preparation thereof | |
| US4667043A (en) | Intermediates for the production of picropodophyllin and related compounds and processes for the preparation and use thereof | |
| JPS57126427A (en) | Preparation of 1-substituted-azulene derivative | |
| KR910000481B1 (ko) | 피리딘 유도체의 제조방법 | |
| JPS5524117A (en) | Preparation of 2-(3-benzoylphenyl) propionic acid | |
| CS195615B1 (en) | Method of producing derivatives of 3-hydroxy-2-phenylpropionic acid | |
| JPS5780367A (en) | Preparation of tryptophan and its derivative |