JPS5953256B2 - α↑１−ｔｅｒｔ．−ブチルアミノメチル−４−ヒドロキシ−ｍ−キシレン−α↑１，α↑３−ジオ−ルの製造法 - Google Patents
α↑１−ｔｅｒｔ．−ブチルアミノメチル−４−ヒドロキシ−ｍ−キシレン−α↑１，α↑３−ジオ−ルの製造法Info
- Publication number
- JPS5953256B2 JPS5953256B2 JP49118004A JP11800474A JPS5953256B2 JP S5953256 B2 JPS5953256 B2 JP S5953256B2 JP 49118004 A JP49118004 A JP 49118004A JP 11800474 A JP11800474 A JP 11800474A JP S5953256 B2 JPS5953256 B2 JP S5953256B2
- Authority
- JP
- Japan
- Prior art keywords
- formula
- tert
- butylaminomethyl
- xylene
- hydroxy
- 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
- 238000004519 manufacturing process Methods 0.000 title claims description 4
- 150000001875 compounds Chemical class 0.000 claims description 14
- 238000005984 hydrogenation reaction Methods 0.000 claims description 9
- 125000005002 aryl methyl group Chemical group 0.000 claims description 5
- 238000009903 catalytic hydrogenation reaction Methods 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 125000006239 protecting group Chemical group 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 238000000034 method Methods 0.000 description 28
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 15
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 14
- 150000002466 imines Chemical class 0.000 description 14
- 239000000047 product Substances 0.000 description 11
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 10
- JPJALAQPGMAKDF-UHFFFAOYSA-N selenium dioxide Chemical compound O=[Se]=O JPJALAQPGMAKDF-UHFFFAOYSA-N 0.000 description 10
- 239000011541 reaction mixture Substances 0.000 description 9
- 239000002904 solvent Substances 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 7
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 6
- -1 lithium aluminum hydride Chemical compound 0.000 description 6
- 229910052711 selenium Inorganic materials 0.000 description 6
- 239000011669 selenium Substances 0.000 description 6
- 238000009835 boiling Methods 0.000 description 5
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 5
- LEQAOMBKQFMDFZ-UHFFFAOYSA-N glyoxal Chemical class O=CC=O LEQAOMBKQFMDFZ-UHFFFAOYSA-N 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- CGKRFDXHYBJWPO-UHFFFAOYSA-N C(C)[AlH]CC.[Na] Chemical compound C(C)[AlH]CC.[Na] CGKRFDXHYBJWPO-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- JEDZLBFUGJTJGQ-UHFFFAOYSA-N [Na].COCCO[AlH]OCCOC Chemical compound [Na].COCCO[AlH]OCCOC JEDZLBFUGJTJGQ-UHFFFAOYSA-N 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 125000004494 ethyl ester group Chemical group 0.000 description 4
- 238000001704 evaporation Methods 0.000 description 4
- 239000000543 intermediate Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000012419 sodium bis(2-methoxyethoxy)aluminum hydride Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 239000013067 intermediate product Substances 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 125000000468 ketone group Chemical group 0.000 description 2
- 239000012280 lithium aluminium hydride Substances 0.000 description 2
- 150000004702 methyl esters Chemical class 0.000 description 2
- IOHPVZBSOKLVMN-UHFFFAOYSA-N 2-(2-phenylethyl)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1CCC1=CC=CC=C1 IOHPVZBSOKLVMN-UHFFFAOYSA-N 0.000 description 1
- VRJBEVQGJOSGOX-UHFFFAOYSA-N 2-acetyloxy-5-bromobenzoic acid Chemical compound CC(=O)OC1=CC=C(Br)C=C1C(O)=O VRJBEVQGJOSGOX-UHFFFAOYSA-N 0.000 description 1
- GMOYUTKNPLBTMT-UHFFFAOYSA-N 2-phenylmethoxybenzoic acid Chemical compound OC(=O)C1=CC=CC=C1OCC1=CC=CC=C1 GMOYUTKNPLBTMT-UHFFFAOYSA-N 0.000 description 1
- NZRDKNBIPVLNHA-UHFFFAOYSA-N 5-Acetylsalicylic acid Chemical group CC(=O)C1=CC=C(O)C(C(O)=O)=C1 NZRDKNBIPVLNHA-UHFFFAOYSA-N 0.000 description 1
- 208000009079 Bronchial Spasm Diseases 0.000 description 1
- 208000014181 Bronchial disease Diseases 0.000 description 1
- 206010006482 Bronchospasm Diseases 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229930194542 Keto Natural products 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
- 239000012670 alkaline solution Substances 0.000 description 1
- DNEHKUCSURWDGO-UHFFFAOYSA-N aluminum sodium Chemical compound [Na].[Al] DNEHKUCSURWDGO-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- ZYBWTEQKHIADDQ-UHFFFAOYSA-N ethanol;methanol Chemical compound OC.CCO ZYBWTEQKHIADDQ-UHFFFAOYSA-N 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000004678 hydrides Chemical class 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000002594 sorbent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 150000003613 toluenes Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/46—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C215/56—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains further substituted by hydroxy groups
- C07C215/58—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains further substituted by hydroxy groups with hydroxy groups and the six-membered aromatic ring, or the condensed ring system containing that ring, bound to the same carbon atom of the carbon chain
- C07C215/60—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains further substituted by hydroxy groups with hydroxy groups and the six-membered aromatic ring, or the condensed ring system containing that ring, bound to the same carbon atom of the carbon chain the chain having two carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
-
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FI982/74A FI56673C (fi) | 1974-03-29 | 1974-03-29 | Nytt foerfarande foer framstaellning av alfa-tert-bytylaminometyl-4-hydroxy-m-xylen-alfa1 alfa3-diol |
| FI98274 | 1974-03-29 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS50130732A JPS50130732A (sv) | 1975-10-16 |
| JPS5953256B2 true JPS5953256B2 (ja) | 1984-12-24 |
Family
ID=8504919
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP49118004A Expired JPS5953256B2 (ja) | 1974-03-29 | 1974-10-14 | α↑１−ｔｅｒｔ．−ブチルアミノメチル−４−ヒドロキシ−ｍ−キシレン−α↑１，α↑３−ジオ−ルの製造法 |
Country Status (7)
| Country | Link |
|---|---|
| JP (1) | JPS5953256B2 (sv) |
| CA (1) | CA1040658A (sv) |
| DK (1) | DK135500C (sv) |
| FI (1) | FI56673C (sv) |
| NO (1) | NO140297C (sv) |
| SE (1) | SE433608B (sv) |
| SU (1) | SU538660A3 (sv) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CY1273A (en) | 1980-07-09 | 1985-03-08 | Draco Ab | 1-(dihydroxyphenyl)-2-amino-ethanol derivatives;preparation,compositions and intermediates |
| FI118418B (sv) | 2003-04-17 | 2007-11-15 | Ecocat Oy | Alumingrundad katalyt för rengöring av gasutskott |
| EP1641741A1 (en) | 2004-05-20 | 2006-04-05 | Teva Pharmaceutical Fine Chemicals S.R.L. | Levalbuterol hydrochloride polymorph b |
| CN110963929B (zh) * | 2019-11-26 | 2022-10-21 | 安徽恒星制药有限公司 | 一种适合工业化生产的盐酸沙丁胺醇制备方法 |
-
1974
- 1974-03-29 FI FI982/74A patent/FI56673C/fi active
- 1974-08-06 SU SU2051832A patent/SU538660A3/ru active
- 1974-10-14 JP JP49118004A patent/JPS5953256B2/ja not_active Expired
-
1975
- 1975-03-25 NO NO751034A patent/NO140297C/no unknown
- 1975-03-26 DK DK133975A patent/DK135500C/da not_active IP Right Cessation
- 1975-03-27 SE SE7503657A patent/SE433608B/sv not_active IP Right Cessation
- 1975-03-27 CA CA223,245A patent/CA1040658A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| SU538660A3 (ru) | 1976-12-05 |
| FI98274A (en) | 1975-09-30 |
| SE433608B (sv) | 1984-06-04 |
| NO751034L (sv) | 1975-09-30 |
| NO140297C (no) | 1979-08-08 |
| FI56673C (fi) | 1981-02-04 |
| DK135500C (da) | 1977-10-24 |
| CA1040658A (en) | 1978-10-17 |
| JPS50130732A (sv) | 1975-10-16 |
| NO140297B (no) | 1979-04-30 |
| DK133975A (sv) | 1975-09-30 |
| FI56673B (fi) | 1979-11-30 |
| DK135500B (da) | 1977-05-09 |
| SE7503657L (sv) | 1975-09-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PL163884B1 (pl) | Sposób wytwarzania fluoksetyny PL PL PL | |
| US2661373A (en) | Certain amino alcohols and ketones | |
| JPS5951956B2 (ja) | ９−ヒドロキシエリプチシン誘導体の合成方法 | |
| CA1118431A (en) | Process for the preparation of cis(.sup. -)-3,4- dihydro-n,n,2-trimethyl-2h-1-benzopyran-3-amine and intermediates produced thereby | |
| SU562196A3 (ru) | Способ получени производных декагидроизохинолина | |
| JPS5953256B2 (ja) | α↑１−ｔｅｒｔ．−ブチルアミノメチル−４−ヒドロキシ−ｍ−キシレン−α↑１，α↑３−ジオ−ルの製造法 | |
| JPS6159316B2 (sv) | ||
| NO750412L (sv) | ||
| US3048633A (en) | N-lower alkyl-2-(benzyloxatedphenyl)-glycolamide | |
| Nakano et al. | Structure of lindenianine from Lupinus lindenianus | |
| US2778832A (en) | Reduction of codeinone to codeine | |
| US3968163A (en) | Preparation of 4 and 5-methylindanes | |
| US3281469A (en) | Process for preparing 5-hydroxy-5-(3-aminoalkynyl) dibenzo [a, d] cyclohepta [1, 4] denes | |
| US3325544A (en) | 9-(2-amino-1-methylethyl) fluoren-9-ol and salts thereof | |
| JP3175339B2 (ja) | 光学活性アミン化合物、その製法、その中間体及びその用途 | |
| CN108840788B (zh) | 一种白藜芦醇的制备方法 | |
| CN117682980B (zh) | 一种2-乙酰基四氢吡啶的制备方法 | |
| US3213128A (en) | Demethylation process | |
| US2797222A (en) | Preparation of neopine | |
| US3694463A (en) | 3-vinyl-cyclo penta (fm{11 )benzopyrans | |
| KR800000542B1 (ko) | 아미노-페닐-에탄올아민의 제조방법 | |
| Smith et al. | 3, 3, 5, 6, 7-Pentamethylhydrindone and 4, 4, 5, 6, 8-Pentamethylhydrocarbostyril | |
| US2528001A (en) | Process of preparing 15-carboxydehydroequilenin compounds, and products of such process | |
| JPH07507286A (ja) | エセレトールの製造方法 | |
| JPS6136262A (ja) | ピペリジノ−プロパノンもしくは−プロパノール誘導体及びその製法 |