FI61310C - Nytt foerfarande foer framstaellning av saosom ett laekemedel anvaendbar 5-metyl-1-fenyl-1,3,4,6-tetrahydro-5h-bens(f)-2,5-oxazocin - Google Patents
Nytt foerfarande foer framstaellning av saosom ett laekemedel anvaendbar 5-metyl-1-fenyl-1,3,4,6-tetrahydro-5h-bens(f)-2,5-oxazocin Download PDFInfo
- Publication number
- FI61310C FI61310C FI760573A FI760573A FI61310C FI 61310 C FI61310 C FI 61310C FI 760573 A FI760573 A FI 760573A FI 760573 A FI760573 A FI 760573A FI 61310 C FI61310 C FI 61310C
- Authority
- FI
- Finland
- Prior art keywords
- tetrahydro
- phenyl
- methyl
- oxazocine
- anvaendbar
- Prior art date
Links
- 238000000034 method Methods 0.000 claims description 13
- 229910000039 hydrogen halide Inorganic materials 0.000 claims description 11
- 239000012433 hydrogen halide Substances 0.000 claims description 11
- 239000011541 reaction mixture Substances 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 8
- QILSFLSDHQAZET-UHFFFAOYSA-N diphenylmethanol Chemical class C=1C=CC=CC=1C(O)C1=CC=CC=C1 QILSFLSDHQAZET-UHFFFAOYSA-N 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- 230000002378 acidificating effect Effects 0.000 claims description 4
- 239000012442 inert solvent Substances 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 14
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000002904 solvent Substances 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000007363 ring formation reaction Methods 0.000 description 5
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 230000035484 reaction time Effects 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- -1 benzhydrol compound Chemical class 0.000 description 3
- 239000012458 free base Substances 0.000 description 3
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 3
- 239000012074 organic phase Substances 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 2
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 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
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- SOHFZNPURCJGEY-UHFFFAOYSA-N 4,1-benzoxazonine Chemical class C1=COC=CC=C2C=CC=CC2=N1 SOHFZNPURCJGEY-UHFFFAOYSA-N 0.000 description 1
- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 108091007369 NEUR proteins Proteins 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
- 239000013543 active substance Substances 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 238000010533 azeotropic distillation Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- IQFVPQOLBLOTPF-HKXUKFGYSA-L congo red Chemical compound [Na+].[Na+].C1=CC=CC2=C(N)C(/N=N/C3=CC=C(C=C3)C3=CC=C(C=C3)/N=N/C3=C(C4=CC=CC=C4C(=C3)S([O-])(=O)=O)N)=CC(S([O-])(=O)=O)=C21 IQFVPQOLBLOTPF-HKXUKFGYSA-L 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D267/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D267/22—Eight-membered rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US55631575 | 1975-03-07 | ||
| US05/556,315 US3978085A (en) | 1975-03-07 | 1975-03-07 | Process for benz[f]-2,5-oxazocines |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI760573A7 FI760573A7 (en, 2012) | 1976-09-08 |
| FI61310B FI61310B (fi) | 1982-03-31 |
| FI61310C true FI61310C (fi) | 1982-07-12 |
Family
ID=24220811
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI760573A FI61310C (fi) | 1975-03-07 | 1976-03-05 | Nytt foerfarande foer framstaellning av saosom ett laekemedel anvaendbar 5-metyl-1-fenyl-1,3,4,6-tetrahydro-5h-bens(f)-2,5-oxazocin |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US3978085A (en, 2012) |
| JP (1) | JPS51113889A (en, 2012) |
| AR (1) | AR211856A1 (en, 2012) |
| AT (1) | AT351548B (en, 2012) |
| AU (1) | AU510010B2 (en, 2012) |
| BE (1) | BE839252A (en, 2012) |
| CA (1) | CA1058615A (en, 2012) |
| CH (1) | CH616416A5 (en, 2012) |
| CS (1) | CS186732B2 (en, 2012) |
| DE (1) | DE2609015C2 (en, 2012) |
| DK (1) | DK142283B (en, 2012) |
| ES (1) | ES445556A1 (en, 2012) |
| FI (1) | FI61310C (en, 2012) |
| FR (1) | FR2303007A1 (en, 2012) |
| GB (1) | GB1545872A (en, 2012) |
| IL (1) | IL49160A (en, 2012) |
| MX (1) | MX3577E (en, 2012) |
| NL (1) | NL7601985A (en, 2012) |
| NO (1) | NO145138C (en, 2012) |
| PH (1) | PH12176A (en, 2012) |
| SE (1) | SE427929B (en, 2012) |
| ZA (1) | ZA76183B (en, 2012) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4208349A (en) * | 1978-07-27 | 1980-06-17 | Riker Laboratories, Inc. | Process for the preparation of 2-[N-(2-hydroxyethyl)-N-lower alkylaminomethyl]benzhydrols |
| US4626522A (en) * | 1980-01-17 | 1986-12-02 | John Wyeth & Brother Limited | Benzoxazocines intermediates |
| US4318909A (en) * | 1980-01-17 | 1982-03-09 | John Wyeth & Brother Limited | Benzoxazocines |
| US20060019940A1 (en) * | 2002-12-20 | 2006-01-26 | Baxter Andrew D | Novel benzoxazocines and their therapeutic use |
| BR0317467A (pt) * | 2002-12-20 | 2005-11-16 | Arakis Ltd | Benzoxazocinas e seu uso como inibidores de reassimilação de monoaminas |
| AU2005235786A1 (en) * | 2004-04-21 | 2005-11-03 | Sosei R&D Ltd. | Benzoxazocines and their therapeutic use as monoamine reuptake inhibitors |
| CN102363610A (zh) * | 2011-11-01 | 2012-02-29 | 安徽万和制药有限公司 | 一种合成盐酸奈福泮的新方法 |
| CN107556263A (zh) * | 2016-06-30 | 2018-01-09 | 康普药业股份有限公司 | 一种盐酸奈福泮的制备方法 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA863349A (en) * | 1971-02-09 | Riker Laboratories, Inc. | Heterocyclic compounds |
-
1975
- 1975-03-07 US US05/556,315 patent/US3978085A/en not_active Expired - Lifetime
-
1976
- 1976-01-13 ZA ZA00760183A patent/ZA76183B/xx unknown
- 1976-02-11 CA CA245,538A patent/CA1058615A/en not_active Expired
- 1976-02-26 NL NL7601985A patent/NL7601985A/xx not_active Application Discontinuation
- 1976-02-26 DK DK83376AA patent/DK142283B/da unknown
- 1976-02-26 NO NO760656A patent/NO145138C/no unknown
- 1976-02-26 SE SE7602449A patent/SE427929B/xx unknown
- 1976-02-26 ES ES445556A patent/ES445556A1/es not_active Expired
- 1976-03-01 CH CH252976A patent/CH616416A5/de not_active IP Right Cessation
- 1976-03-04 DE DE2609015A patent/DE2609015C2/de not_active Expired
- 1976-03-05 JP JP51024042A patent/JPS51113889A/ja active Pending
- 1976-03-05 PH PH18179A patent/PH12176A/en unknown
- 1976-03-05 IL IL49160A patent/IL49160A/xx unknown
- 1976-03-05 BE BE164904A patent/BE839252A/xx not_active IP Right Cessation
- 1976-03-05 FI FI760573A patent/FI61310C/fi not_active IP Right Cessation
- 1976-03-05 AR AR262450A patent/AR211856A1/es active
- 1976-03-05 AU AU11705/76A patent/AU510010B2/en not_active Expired
- 1976-03-05 FR FR7606418A patent/FR2303007A1/fr active Granted
- 1976-03-05 CS CS7600001466A patent/CS186732B2/cs unknown
- 1976-03-05 MX MX7645U patent/MX3577E/es unknown
- 1976-03-05 AT AT164476A patent/AT351548B/de not_active IP Right Cessation
- 1976-03-08 GB GB9209/76A patent/GB1545872A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| ATA164476A (de) | 1979-01-15 |
| NO145138C (no) | 1982-01-20 |
| FR2303007A1 (fr) | 1976-10-01 |
| FI61310B (fi) | 1982-03-31 |
| CS186732B2 (en) | 1978-12-29 |
| JPS51113889A (en) | 1976-10-07 |
| IL49160A (en) | 1979-01-31 |
| CA1058615A (en) | 1979-07-17 |
| NO145138B (no) | 1981-10-12 |
| AU510010B2 (en) | 1980-06-05 |
| DE2609015C2 (de) | 1986-05-07 |
| CH616416A5 (en, 2012) | 1980-03-31 |
| US3978085A (en) | 1976-08-31 |
| DK142283B (da) | 1980-10-06 |
| FR2303007B1 (en, 2012) | 1980-02-08 |
| AU1170576A (en) | 1977-09-08 |
| SE7602449L (sv) | 1976-09-08 |
| ZA76183B (en) | 1976-12-29 |
| DK83376A (en, 2012) | 1976-09-08 |
| AR211856A1 (es) | 1978-03-31 |
| MX3577E (es) | 1981-03-19 |
| SE427929B (sv) | 1983-05-24 |
| BE839252A (fr) | 1976-09-06 |
| NO760656L (en, 2012) | 1976-09-08 |
| DK142283C (en, 2012) | 1981-03-02 |
| GB1545872A (en) | 1979-05-16 |
| PH12176A (en) | 1978-11-21 |
| NL7601985A (nl) | 1976-09-09 |
| AT351548B (de) | 1979-07-25 |
| DE2609015A1 (de) | 1976-09-16 |
| FI760573A7 (en, 2012) | 1976-09-08 |
| IL49160A0 (en) | 1976-05-31 |
| ES445556A1 (es) | 1977-06-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed |
Owner name: RIKER LABORATORIES, INC. |