ZA200100526B - Process for producing 2-aminobenzophenone compound. - Google Patents
Process for producing 2-aminobenzophenone compound. Download PDFInfo
- Publication number
- ZA200100526B ZA200100526B ZA200100526A ZA200100526A ZA200100526B ZA 200100526 B ZA200100526 B ZA 200100526B ZA 200100526 A ZA200100526 A ZA 200100526A ZA 200100526 A ZA200100526 A ZA 200100526A ZA 200100526 B ZA200100526 B ZA 200100526B
- Authority
- ZA
- South Africa
- Prior art keywords
- reaction
- acid
- formula
- producing
- represented
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 12
- -1 2-aminobenzophenone compound Chemical class 0.000 title description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 20
- MAOBFOXLCJIFLV-UHFFFAOYSA-N (2-aminophenyl)-phenylmethanone Chemical compound NC1=CC=CC=C1C(=O)C1=CC=CC=C1 MAOBFOXLCJIFLV-UHFFFAOYSA-N 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000004421 aryl sulphonamide group Chemical group 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 description 21
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 8
- 238000011445 neoadjuvant hormone therapy Methods 0.000 description 8
- 238000005881 detosylation reaction Methods 0.000 description 7
- RWZYAGGXGHYGMB-UHFFFAOYSA-N anthranilic acid Chemical compound NC1=CC=CC=C1C(O)=O RWZYAGGXGHYGMB-UHFFFAOYSA-N 0.000 description 6
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 4
- ADALGBTXGIISDM-UHFFFAOYSA-N 2-[(4-methylphenyl)sulfonylamino]benzoic acid Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC1=CC=CC=C1C(O)=O ADALGBTXGIISDM-UHFFFAOYSA-N 0.000 description 4
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 239000000543 intermediate Substances 0.000 description 4
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 3
- 235000012000 cholesterol Nutrition 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 229940121710 HMGCoA reductase inhibitor Drugs 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 239000002260 anti-inflammatory agent Substances 0.000 description 2
- 229940121363 anti-inflammatory agent Drugs 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000002471 hydroxymethylglutaryl coenzyme A reductase inhibitor Substances 0.000 description 2
- 238000004811 liquid chromatography Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 208000020016 psychiatric disease Diseases 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- FFFXIQFESQNINT-UHFFFAOYSA-N (2-aminophenyl)-(4-fluorophenyl)methanone Chemical compound NC1=CC=CC=C1C(=O)C1=CC=C(F)C=C1 FFFXIQFESQNINT-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 102000004316 Oxidoreductases Human genes 0.000 description 1
- 108090000854 Oxidoreductases Proteins 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- SMWDFEZZVXVKRB-UHFFFAOYSA-N anhydrous quinoline Natural products N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- YKGMKSIHIVVYKY-UHFFFAOYSA-N dabrafenib mesylate Chemical compound CS(O)(=O)=O.S1C(C(C)(C)C)=NC(C=2C(=C(NS(=O)(=O)C=3C(=CC=CC=3F)F)C=CC=2)F)=C1C1=CC=NC(N)=N1 YKGMKSIHIVVYKY-UHFFFAOYSA-N 0.000 description 1
- 238000010511 deprotection reaction Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- PYLWMHQQBFSUBP-UHFFFAOYSA-N monofluorobenzene Chemical compound FC1=CC=CC=C1 PYLWMHQQBFSUBP-UHFFFAOYSA-N 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- UHZYTMXLRWXGPK-UHFFFAOYSA-N phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C221/00—Preparation of compounds containing amino groups and doubly-bound oxygen atoms bound to the same carbon skeleton
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Hematology (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Psychiatry (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP20791098 | 1998-07-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200100526B true ZA200100526B (en) | 2001-08-02 |
Family
ID=16547602
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200100526A ZA200100526B (en) | 1998-07-23 | 2001-01-18 | Process for producing 2-aminobenzophenone compound. |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US6310249B1 (cs) |
| EP (1) | EP1099687B1 (cs) |
| JP (1) | JP4232337B2 (cs) |
| KR (1) | KR100594339B1 (cs) |
| CN (1) | CN1131204C (cs) |
| AT (1) | ATE259347T1 (cs) |
| AU (1) | AU746711B2 (cs) |
| CA (1) | CA2338421C (cs) |
| CZ (1) | CZ300228B6 (cs) |
| DE (1) | DE69914763T2 (cs) |
| DK (1) | DK1099687T3 (cs) |
| ES (1) | ES2216533T3 (cs) |
| IL (1) | IL140925A0 (cs) |
| NO (1) | NO317811B1 (cs) |
| NZ (1) | NZ509399A (cs) |
| PT (1) | PT1099687E (cs) |
| RU (1) | RU2223945C2 (cs) |
| SK (1) | SK286961B6 (cs) |
| UA (1) | UA58601C2 (cs) |
| WO (1) | WO2000005195A1 (cs) |
| ZA (1) | ZA200100526B (cs) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101270060B (zh) * | 2008-05-07 | 2011-02-02 | 重庆医科大学 | 2，6-二（氨基苯亚甲基）环烷酮类化合物及其制备方法和用途 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB332208A (en) * | 1929-01-15 | 1930-07-15 | Ig Farbenindustrie Ag | Process for the manufacture of azo dyestuffs |
| US3297755A (en) * | 1960-12-02 | 1967-01-10 | Hoffmann La Roche | 2-chloro-5-trifluoromethylbenzo-phenone compounds |
| BE622079A (cs) * | 1961-09-11 | |||
| DE69303996T2 (de) * | 1992-07-06 | 1997-02-27 | American Cyanamid Co | o-Nitrophenyl Cyclopropyl Keton, herbizides Zwischenprodukt und Verfahren zu seiner Herstellung |
| CZ289916B6 (cs) * | 1993-11-30 | 2002-04-17 | American Cyanamid Company | Způsob výroby o-aminofenylketonů |
-
1999
- 1999-07-22 DK DK99931483T patent/DK1099687T3/da active
- 1999-07-22 CN CN99808967A patent/CN1131204C/zh not_active Expired - Fee Related
- 1999-07-22 DE DE69914763T patent/DE69914763T2/de not_active Expired - Lifetime
- 1999-07-22 WO PCT/JP1999/003922 patent/WO2000005195A1/ja active IP Right Grant
- 1999-07-22 PT PT99931483T patent/PT1099687E/pt unknown
- 1999-07-22 EP EP99931483A patent/EP1099687B1/en not_active Expired - Lifetime
- 1999-07-22 ES ES99931483T patent/ES2216533T3/es not_active Expired - Lifetime
- 1999-07-22 US US09/743,810 patent/US6310249B1/en not_active Expired - Lifetime
- 1999-07-22 KR KR1020017000688A patent/KR100594339B1/ko not_active Expired - Fee Related
- 1999-07-22 RU RU2001105198/04A patent/RU2223945C2/ru not_active IP Right Cessation
- 1999-07-22 CZ CZ20010063A patent/CZ300228B6/cs not_active IP Right Cessation
- 1999-07-22 SK SK63-2001A patent/SK286961B6/sk not_active IP Right Cessation
- 1999-07-22 JP JP2000561152A patent/JP4232337B2/ja not_active Expired - Fee Related
- 1999-07-22 NZ NZ509399A patent/NZ509399A/en not_active IP Right Cessation
- 1999-07-22 IL IL14092599A patent/IL140925A0/xx not_active IP Right Cessation
- 1999-07-22 AT AT99931483T patent/ATE259347T1/de active
- 1999-07-22 AU AU47991/99A patent/AU746711B2/en not_active Ceased
- 1999-07-22 UA UA2001010586A patent/UA58601C2/uk unknown
- 1999-07-22 CA CA002338421A patent/CA2338421C/en not_active Expired - Fee Related
-
2001
- 2001-01-18 ZA ZA200100526A patent/ZA200100526B/en unknown
- 2001-01-22 NO NO20010356A patent/NO317811B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| JP4232337B2 (ja) | 2009-03-04 |
| ATE259347T1 (de) | 2004-02-15 |
| CN1131204C (zh) | 2003-12-17 |
| NO20010356L (no) | 2001-01-22 |
| CN1310703A (zh) | 2001-08-29 |
| RU2223945C2 (ru) | 2004-02-20 |
| NO20010356D0 (no) | 2001-01-22 |
| WO2000005195A1 (fr) | 2000-02-03 |
| SK632001A3 (en) | 2001-08-06 |
| KR100594339B1 (ko) | 2006-06-30 |
| CZ300228B6 (cs) | 2009-03-25 |
| SK286961B6 (sk) | 2009-08-06 |
| ES2216533T3 (es) | 2004-10-16 |
| EP1099687A4 (en) | 2003-01-02 |
| IL140925A0 (en) | 2002-02-10 |
| UA58601C2 (uk) | 2003-08-15 |
| NZ509399A (en) | 2002-03-01 |
| AU746711B2 (en) | 2002-05-02 |
| EP1099687B1 (en) | 2004-02-11 |
| EP1099687A1 (en) | 2001-05-16 |
| DE69914763D1 (de) | 2004-03-18 |
| PT1099687E (pt) | 2004-06-30 |
| CA2338421C (en) | 2007-05-08 |
| KR20010071938A (ko) | 2001-07-31 |
| NO317811B1 (no) | 2004-12-13 |
| US6310249B1 (en) | 2001-10-30 |
| AU4799199A (en) | 2000-02-14 |
| DE69914763T2 (de) | 2004-07-15 |
| DK1099687T3 (da) | 2004-04-13 |
| CA2338421A1 (en) | 2000-02-03 |
| CZ200163A3 (en) | 2001-06-13 |
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