NO333493B1 - Ny fremgangsmate for syntesen av (7-metoksy-1-naftyl)acetonitril og dens anvendelse i syntesen av agomelatin - Google Patents
Ny fremgangsmate for syntesen av (7-metoksy-1-naftyl)acetonitril og dens anvendelse i syntesen av agomelatin Download PDFInfo
- Publication number
- NO333493B1 NO333493B1 NO20050739A NO20050739A NO333493B1 NO 333493 B1 NO333493 B1 NO 333493B1 NO 20050739 A NO20050739 A NO 20050739A NO 20050739 A NO20050739 A NO 20050739A NO 333493 B1 NO333493 B1 NO 333493B1
- Authority
- NO
- Norway
- Prior art keywords
- compound
- synthesis
- formula
- methoxy
- acetonitrile
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 20
- 230000015572 biosynthetic process Effects 0.000 title claims abstract description 17
- 238000003786 synthesis reaction Methods 0.000 title claims abstract description 17
- YJYPHIXNFHFHND-UHFFFAOYSA-N agomelatine Chemical compound C1=CC=C(CCNC(C)=O)C2=CC(OC)=CC=C21 YJYPHIXNFHFHND-UHFFFAOYSA-N 0.000 title claims abstract description 14
- 229960002629 agomelatine Drugs 0.000 title claims abstract description 11
- PYJMGUQHJINLLD-UHFFFAOYSA-N 2-(7-methoxynaphthalen-1-yl)acetonitrile Chemical compound C1=CC=C(CC#N)C2=CC(OC)=CC=C21 PYJMGUQHJINLLD-UHFFFAOYSA-N 0.000 title description 7
- 150000001875 compounds Chemical class 0.000 claims abstract description 18
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 18
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical group [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 16
- 239000003054 catalyst Substances 0.000 claims description 10
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 claims description 6
- -1 allyl compound Chemical class 0.000 claims description 6
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 238000005984 hydrogenation reaction Methods 0.000 claims description 6
- 238000010992 reflux Methods 0.000 claims description 6
- 239000000758 substrate Substances 0.000 claims description 4
- MGJHVZKRAOYORH-UHFFFAOYSA-N 2-(7-methoxy-3,4-dihydronaphthalen-1-yl)acetonitrile Chemical compound C1CC=C(CC#N)C2=CC(OC)=CC=C21 MGJHVZKRAOYORH-UHFFFAOYSA-N 0.000 claims description 3
- 238000001704 evaporation Methods 0.000 claims description 3
- 230000008020 evaporation Effects 0.000 claims description 3
- 229910052763 palladium Inorganic materials 0.000 claims description 3
- 239000007787 solid Substances 0.000 claims description 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 230000008878 coupling Effects 0.000 claims description 2
- 238000010168 coupling process Methods 0.000 claims description 2
- 238000005859 coupling reaction Methods 0.000 claims description 2
- 238000001914 filtration Methods 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 238000001953 recrystallisation Methods 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 238000001308 synthesis method Methods 0.000 claims 1
- HZNVUJQVZSTENZ-UHFFFAOYSA-N 2,3-dichloro-5,6-dicyano-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(C#N)=C(C#N)C1=O HZNVUJQVZSTENZ-UHFFFAOYSA-N 0.000 description 6
- GABLTKRIYDNDIN-UHFFFAOYSA-N 7-methoxy-3,4-dihydro-2h-naphthalen-1-one Chemical compound C1CCC(=O)C2=CC(OC)=CC=C21 GABLTKRIYDNDIN-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 238000005899 aromatization reaction Methods 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 230000018044 dehydration Effects 0.000 description 2
- HMCZXRUEDOKTLT-UHFFFAOYSA-N ethyl 2-(7-methoxy-3,4-dihydro-2h-naphthalen-1-ylidene)acetate Chemical compound C1=C(OC)C=C2C(=CC(=O)OCC)CCCC2=C1 HMCZXRUEDOKTLT-UHFFFAOYSA-N 0.000 description 2
- PQJJJMRNHATNKG-UHFFFAOYSA-N ethyl bromoacetate Chemical compound CCOC(=O)CBr PQJJJMRNHATNKG-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000007170 pathology Effects 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 2
- QTECDUFMBMSHKR-UHFFFAOYSA-N prop-2-enyl prop-2-enoate Chemical compound C=CCOC(=O)C=C QTECDUFMBMSHKR-UHFFFAOYSA-N 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 238000007127 saponification reaction Methods 0.000 description 2
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 208000027559 Appetite disease Diseases 0.000 description 1
- 208000019888 Circadian rhythm sleep disease Diseases 0.000 description 1
- 208000019454 Feeding and Eating disease Diseases 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 208000001456 Jet Lag Syndrome Diseases 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 208000008589 Obesity Diseases 0.000 description 1
- 208000013738 Sleep Initiation and Maintenance disease Diseases 0.000 description 1
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
- 239000012346 acetyl chloride Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000556 agonist Substances 0.000 description 1
- 239000005557 antagonist Substances 0.000 description 1
- 210000003169 central nervous system Anatomy 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 210000002249 digestive system Anatomy 0.000 description 1
- 230000002526 effect on cardiovascular system Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000009776 industrial production Methods 0.000 description 1
- 206010022437 insomnia Diseases 0.000 description 1
- 208000033915 jet lag type circadian rhythm sleep disease Diseases 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000001193 melatoninergic effect Effects 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000003822 preparative gas chromatography Methods 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 208000012672 seasonal affective disease Diseases 0.000 description 1
- 208000019116 sleep disease Diseases 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/30—Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/24—Surgical instruments, devices or methods, e.g. tourniquets for use in the oral cavity, larynx, bronchial passages or nose; Tongue scrapers
- A61B17/244—Surgical instruments, devices or methods, e.g. tourniquets for use in the oral cavity, larynx, bronchial passages or nose; Tongue scrapers for cleaning of the tongue
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61C—DENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
- A61C17/00—Devices for cleaning, polishing, rinsing or drying teeth, teeth cavities or prostheses; Saliva removers; Dental appliances for receiving spittle
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0401437A FR2866337B1 (fr) | 2004-02-13 | 2004-02-13 | Nouveau procede de synthese du (7-methoxy-1-naphtyl) acetonitrile et application a la synthese de l'aglomelatine |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20050739D0 NO20050739D0 (no) | 2005-02-11 |
| NO20050739L NO20050739L (no) | 2005-08-15 |
| NO333493B1 true NO333493B1 (no) | 2013-06-24 |
Family
ID=34685017
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20050739A NO333493B1 (no) | 2004-02-13 | 2005-02-11 | Ny fremgangsmate for syntesen av (7-metoksy-1-naftyl)acetonitril og dens anvendelse i syntesen av agomelatin |
Country Status (33)
| Country | Link |
|---|---|
| US (2) | US7470806B2 (ru) |
| EP (1) | EP1564205B1 (ru) |
| JP (1) | JP4157529B2 (ru) |
| KR (1) | KR100682698B1 (ru) |
| CN (1) | CN1300100C (ru) |
| AR (1) | AR047740A1 (ru) |
| AT (1) | ATE395326T1 (ru) |
| AU (1) | AU2005200615B8 (ru) |
| BR (1) | BRPI0502037B8 (ru) |
| CA (1) | CA2495975A1 (ru) |
| CY (1) | CY1111081T1 (ru) |
| DE (1) | DE602005006634D1 (ru) |
| DK (1) | DK1564205T3 (ru) |
| EA (1) | EA007787B1 (ru) |
| ES (1) | ES2308409T3 (ru) |
| FR (1) | FR2866337B1 (ru) |
| GE (1) | GEP20063929B (ru) |
| HK (1) | HK1078564A1 (ru) |
| HR (1) | HRP20080315T3 (ru) |
| MA (1) | MA27516A1 (ru) |
| ME (1) | ME01403B (ru) |
| MX (1) | MXPA05001636A (ru) |
| MY (1) | MY140089A (ru) |
| NO (1) | NO333493B1 (ru) |
| NZ (1) | NZ538193A (ru) |
| PL (1) | PL1564205T3 (ru) |
| PT (1) | PT1564205E (ru) |
| RS (1) | RS50594B (ru) |
| SG (1) | SG114705A1 (ru) |
| SI (1) | SI1564205T1 (ru) |
| UA (1) | UA79623C2 (ru) |
| WO (1) | WO2005077889A1 (ru) |
| ZA (1) | ZA200501255B (ru) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2580183B1 (en) | 2010-06-10 | 2014-07-23 | Gador S.A. | New process for the preparation of n-[2-(7-methoxy-1-naphthyl)-ethyl]acetamide |
| WO2013054273A2 (en) | 2011-10-11 | 2013-04-18 | Ranbaxy Laboratories Limited | Process for the preparation of agomelatine |
| US20140336380A1 (en) | 2011-12-01 | 2014-11-13 | Ranbaxy Laboratories Limited | Process for the preparation of agomelatine |
| ITMI20121444A1 (it) | 2012-08-27 | 2014-02-28 | Procos Spa | Processo per la produzione di agomelatine |
| FR3014434B1 (fr) * | 2013-12-05 | 2015-12-25 | Servier Lab | Nouveau procede de synthese du 7-methoxy-naphtalene-1-carbaldehyde et application a la synthese de l'agomelatine |
| CN112574066A (zh) * | 2019-09-27 | 2021-03-30 | 江苏豪森药业集团有限公司 | 一种阿戈美拉汀中间体的制备方法 |
| CN111377829A (zh) * | 2020-04-10 | 2020-07-07 | 苏州敬业医药化工有限公司 | 一种7-甲氧基-1-萘乙腈的制备方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4169108A (en) * | 1973-08-16 | 1979-09-25 | Sterling Drug Inc. | 5(OR 6)-[(Substituted-amino)alkyl]-2,3-naphthalenediols |
| US4327022A (en) * | 1973-08-16 | 1982-04-27 | Sterling Drug Inc. | Heterocyclic alkyl naphthols |
| US3931188A (en) * | 1974-05-06 | 1976-01-06 | Bristol-Myers Company | 3-Hydroxy-5,6-benzomorphinan derivatives |
| US3992403A (en) * | 1975-05-30 | 1976-11-16 | Schering Corporation | 2-Imidazolines and their use as hypoglycemic agents |
| FR2658818B1 (fr) * | 1990-02-27 | 1993-12-31 | Adir Cie | Nouveaux derives a structure naphtalenique, leur procede de preparation et les compositions pharmaceutiques qui les contiennent. |
-
2004
- 2004-02-13 FR FR0401437A patent/FR2866337B1/fr not_active Expired - Fee Related
-
2005
- 2005-02-01 CA CA002495975A patent/CA2495975A1/fr not_active Abandoned
- 2005-02-04 US US11/051,868 patent/US7470806B2/en active Active
- 2005-02-07 MY MYPI20050474A patent/MY140089A/en unknown
- 2005-02-07 SG SG200500679A patent/SG114705A1/en unknown
- 2005-02-10 MX MXPA05001636A patent/MXPA05001636A/es active IP Right Grant
- 2005-02-11 RS RSP-2008/0349A patent/RS50594B/sr unknown
- 2005-02-11 NO NO20050739A patent/NO333493B1/no unknown
- 2005-02-11 AR ARP050100500A patent/AR047740A1/es unknown
- 2005-02-11 GE GEAP8623A patent/GEP20063929B/en unknown
- 2005-02-11 BR BRPI0502037A patent/BRPI0502037B8/pt active IP Right Grant
- 2005-02-11 SI SI200530266T patent/SI1564205T1/sl unknown
- 2005-02-11 EP EP05290310A patent/EP1564205B1/fr active Active
- 2005-02-11 UA UAA200501280A patent/UA79623C2/uk unknown
- 2005-02-11 ME MEP-2008-959A patent/ME01403B/me unknown
- 2005-02-11 DK DK05290310T patent/DK1564205T3/da active
- 2005-02-11 ZA ZA2005/01255A patent/ZA200501255B/en unknown
- 2005-02-11 AU AU2005200615A patent/AU2005200615B8/en active Active
- 2005-02-11 ES ES05290310T patent/ES2308409T3/es active Active
- 2005-02-11 NZ NZ538193A patent/NZ538193A/en unknown
- 2005-02-11 WO PCT/FR2005/000325 patent/WO2005077889A1/fr active Application Filing
- 2005-02-11 PT PT05290310T patent/PT1564205E/pt unknown
- 2005-02-11 PL PL05290310T patent/PL1564205T3/pl unknown
- 2005-02-11 AT AT05290310T patent/ATE395326T1/de active
- 2005-02-11 MA MA28099A patent/MA27516A1/fr unknown
- 2005-02-11 DE DE602005006634T patent/DE602005006634D1/de active Active
- 2005-02-12 KR KR1020050011749A patent/KR100682698B1/ko active Protection Beyond IP Right Term
- 2005-02-14 JP JP2005035756A patent/JP4157529B2/ja active Active
- 2005-02-14 EA EA200500204A patent/EA007787B1/ru unknown
- 2005-02-16 CN CNB2005100716239A patent/CN1300100C/zh active Active
- 2005-11-21 HK HK05110485A patent/HK1078564A1/xx unknown
-
2008
- 2008-06-10 CY CY20081100616T patent/CY1111081T1/el unknown
- 2008-07-01 HR HR20080315T patent/HRP20080315T3/xx unknown
- 2008-11-26 US US12/313,921 patent/US7994359B2/en active Active
Also Published As
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| NO333488B1 (no) | Ny fremgangsmate for syntesen av (7-metoksy-1-naftyl)acetonitril og anvendelse i syntesen av agomelatin | |
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| NO333483B1 (no) | Ny fremgangsmate for syntesen av (7-metoksy-3,4-dihydro-1-naftalenyl)acetonitril og dens anvendelse i syntesen av agomelatin | |
| AU2009203052B2 (en) | New process for the synthesis of agomelatine | |
| US7994359B2 (en) | Process for the synthesis of (7-methoxy-1-naphthyl) acetonitrile and its application in the synthesis of agomelatine |