NO136361B - - Google Patents
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- Publication number
- NO136361B NO136361B NO3829/72A NO382972A NO136361B NO 136361 B NO136361 B NO 136361B NO 3829/72 A NO3829/72 A NO 3829/72A NO 382972 A NO382972 A NO 382972A NO 136361 B NO136361 B NO 136361B
- Authority
- NO
- Norway
- Prior art keywords
- alkyl
- stands
- trifluoromethyl
- carbon atoms
- urea
- Prior art date
Links
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 15
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 11
- 239000004202 carbamide Substances 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 8
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 8
- 229960000583 acetic acid Drugs 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000004414 alkyl thio group Chemical group 0.000 claims description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 239000011737 fluorine Substances 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- 239000012362 glacial acetic acid Substances 0.000 claims description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims description 2
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 3
- 150000001735 carboxylic acids Chemical class 0.000 claims 2
- 230000008018 melting Effects 0.000 description 13
- 238000002844 melting Methods 0.000 description 13
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 239000000155 melt Substances 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- JTIGKVIOEQASGT-UHFFFAOYSA-N proquazone Chemical compound N=1C(=O)N(C(C)C)C2=CC(C)=CC=C2C=1C1=CC=CC=C1 JTIGKVIOEQASGT-UHFFFAOYSA-N 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000012965 benzophenone Substances 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000004809 thin layer chromatography Methods 0.000 description 2
- MAOBFOXLCJIFLV-UHFFFAOYSA-N (2-aminophenyl)-phenylmethanone Chemical compound NC1=CC=CC=C1C(=O)C1=CC=CC=C1 MAOBFOXLCJIFLV-UHFFFAOYSA-N 0.000 description 1
- QVHATTMFVNBSBM-UHFFFAOYSA-N 1-ethyl-4-phenyl-6-(trifluoromethyl)quinazolin-2-one Chemical compound N=1C(=O)N(CC)C2=CC=C(C(F)(F)F)C=C2C=1C1=CC=CC=C1 QVHATTMFVNBSBM-UHFFFAOYSA-N 0.000 description 1
- HHTYFUMRSWVPQZ-UHFFFAOYSA-N 1-ethyl-6-nitro-4-phenylquinazolin-2-one Chemical compound N=1C(=O)N(CC)C2=CC=C([N+]([O-])=O)C=C2C=1C1=CC=CC=C1 HHTYFUMRSWVPQZ-UHFFFAOYSA-N 0.000 description 1
- GGQFTYRITULEJT-UHFFFAOYSA-N 1-methyl-4-[3-(trifluoromethyl)phenyl]quinazolin-2-one Chemical compound CN1C(N=C(C2=CC=CC=C12)C1=CC(=CC=C1)C(F)(F)F)=O GGQFTYRITULEJT-UHFFFAOYSA-N 0.000 description 1
- XIKDAYOTILSCHK-UHFFFAOYSA-N 4-(4-chlorophenyl)-1-methylquinazolin-2-one Chemical compound CN1C(N=C(C2=CC=CC=C12)C1=CC=C(C=C1)Cl)=O XIKDAYOTILSCHK-UHFFFAOYSA-N 0.000 description 1
- VVFOHEGARONNBX-UHFFFAOYSA-N 4-(4-methoxyphenyl)-7-methyl-1-propan-2-ylquinazolin-2-one Chemical compound C(C)(C)N1C(N=C(C2=CC=C(C=C12)C)C1=CC=C(C=C1)OC)=O VVFOHEGARONNBX-UHFFFAOYSA-N 0.000 description 1
- UUONGVUQZPZQNV-UHFFFAOYSA-N 4-(4-methylphenyl)-1-propan-2-ylquinazolin-2-one Chemical compound C(C)(C)N1C(N=C(C2=CC=CC=C12)C1=CC=C(C=C1)C)=O UUONGVUQZPZQNV-UHFFFAOYSA-N 0.000 description 1
- JAPCFGJAINHVJK-UHFFFAOYSA-N 5,7-dimethyl-4-phenyl-1-propan-2-ylquinazolin-2-one Chemical compound N=1C(=O)N(C(C)C)C2=CC(C)=CC(C)=C2C=1C1=CC=CC=C1 JAPCFGJAINHVJK-UHFFFAOYSA-N 0.000 description 1
- LDQHRBDVFDKRAR-UHFFFAOYSA-N 6,7-dichloro-4-phenyl-1-propan-2-ylquinazolin-2-one Chemical compound ClC=1C=C2C(=NC(N(C2=CC1Cl)C(C)C)=O)C1=CC=CC=C1 LDQHRBDVFDKRAR-UHFFFAOYSA-N 0.000 description 1
- XWNIPACDYFLORY-UHFFFAOYSA-N 6,7-dimethyl-4-phenyl-1-prop-2-ynylquinazolin-2-one Chemical compound CC=1C=C2C(=NC(N(C2=CC1C)CC#C)=O)C1=CC=CC=C1 XWNIPACDYFLORY-UHFFFAOYSA-N 0.000 description 1
- AYIPUPLLAZJWMR-UHFFFAOYSA-N 6-bromo-4-phenyl-1-propan-2-ylquinazolin-2-one Chemical compound BrC=1C=C2C(=NC(N(C2=CC1)C(C)C)=O)C1=CC=CC=C1 AYIPUPLLAZJWMR-UHFFFAOYSA-N 0.000 description 1
- QGHJRJCNYBJPFL-UHFFFAOYSA-N 6-methoxy-4-phenyl-1-propan-2-ylquinazolin-2-one Chemical compound C12=CC(OC)=CC=C2N(C(C)C)C(=O)N=C1C1=CC=CC=C1 QGHJRJCNYBJPFL-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000908 ammonium hydroxide Substances 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000006798 ring closing metathesis reaction Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/62—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to atoms of the carbocyclic ring
- C07D317/66—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
- C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
- C07D317/62—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to atoms of the carbocyclic ring
- C07D317/68—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US20014171A | 1971-11-18 | 1971-11-18 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO136361B true NO136361B (de) | 1977-05-16 |
| NO136361C NO136361C (no) | 1977-08-24 |
Family
ID=22740499
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO3829/72A NO136361C (no) | 1971-11-18 | 1972-10-25 | Fremgangsm}te for fremstilling av 1-alkyl-4-fenyl-2(1h)-kinazolinoner. |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US3793324A (de) |
| JP (1) | JPS5516424B2 (de) |
| AR (1) | AR200718A1 (de) |
| AT (1) | AT339313B (de) |
| AU (1) | AU472728B2 (de) |
| BE (1) | BE790804A (de) |
| BG (1) | BG26811A3 (de) |
| CA (2) | CA983501A (de) |
| CH (1) | CH574942A5 (de) |
| CS (1) | CS182229B2 (de) |
| DD (1) | DD100950A5 (de) |
| DE (1) | DE2253165A1 (de) |
| DK (1) | DK130972B (de) |
| ES (1) | ES408156A1 (de) |
| FI (1) | FI57402C (de) |
| FR (1) | FR2160385B1 (de) |
| GB (1) | GB1385420A (de) |
| HU (1) | HU165128B (de) |
| IE (1) | IE36968B1 (de) |
| IL (1) | IL40858A (de) |
| NL (1) | NL7214565A (de) |
| NO (1) | NO136361C (de) |
| OA (1) | OA04212A (de) |
| PL (1) | PL85287B1 (de) |
| RO (1) | RO63386A (de) |
| SE (1) | SE412391B (de) |
| SU (1) | SU474985A3 (de) |
| YU (1) | YU36933B (de) |
| ZA (1) | ZA727760B (de) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH625512A5 (de) * | 1976-12-13 | 1981-09-30 | Sandoz Ag | |
| JPS608274A (ja) * | 1983-06-27 | 1985-01-17 | Fujisawa Pharmaceut Co Ltd | 新規キナゾリノン誘導体およびその製造法・並びに抗アレルギ−剤 |
| US4521421A (en) * | 1983-09-26 | 1985-06-04 | Eli Lilly And Company | Treatment of sexual dysfunction |
| AR038658A1 (es) * | 2001-06-15 | 2005-01-26 | Novartis Ag | Derivados de 4-aril-2(1h) quinazolinona y 4-aril-quinazolina 2-sustituidas, un proceso para su preparacion, composiciones farmaceuticas y el uso de dichos derivados para la preparacion de un medicamento |
| GB0230015D0 (en) * | 2002-12-23 | 2003-01-29 | Novartis Ag | Organic compounds |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BG16442A3 (bg) * | 1967-10-30 | 1972-11-20 | Max Denzer | Метод за получаване на нови о-изопропиламинобензофенони |
-
0
- BE BE790804D patent/BE790804A/xx unknown
-
1971
- 1971-11-18 US US00200141A patent/US3793324A/en not_active Expired - Lifetime
-
1972
- 1972-06-22 CA CA145,389A patent/CA983501A/en not_active Expired
- 1972-10-23 CH CH1546972A patent/CH574942A5/xx not_active IP Right Cessation
- 1972-10-24 DK DK526472AA patent/DK130972B/da unknown
- 1972-10-25 FR FR7237751A patent/FR2160385B1/fr not_active Expired
- 1972-10-25 NO NO3829/72A patent/NO136361C/no unknown
- 1972-10-26 SE SE7213849A patent/SE412391B/xx unknown
- 1972-10-26 FI FI2971/72A patent/FI57402C/fi active
- 1972-10-27 NL NL7214565A patent/NL7214565A/xx not_active Application Discontinuation
- 1972-10-30 DE DE2253165A patent/DE2253165A1/de not_active Withdrawn
- 1972-10-30 YU YU2688/72A patent/YU36933B/xx unknown
- 1972-10-31 BG BG7221753A patent/BG26811A3/xx unknown
- 1972-10-31 PL PL1972158570A patent/PL85287B1/pl unknown
- 1972-10-31 CS CS7200007326A patent/CS182229B2/cs unknown
- 1972-10-31 HU HUSA2416A patent/HU165128B/hu unknown
- 1972-10-31 RO RO7200072684A patent/RO63386A/ro unknown
- 1972-10-31 AU AU48360/72A patent/AU472728B2/en not_active Expired
- 1972-10-31 AR AR244903A patent/AR200718A1/es active
- 1972-10-31 ES ES408156A patent/ES408156A1/es not_active Expired
- 1972-10-31 CA CA155,222A patent/CA976165A/en not_active Expired
- 1972-10-31 DD DD166584A patent/DD100950A5/xx unknown
- 1972-10-31 GB GB5010472A patent/GB1385420A/en not_active Expired
- 1972-11-01 ZA ZA727760A patent/ZA727760B/xx unknown
- 1972-11-01 JP JP10893672A patent/JPS5516424B2/ja not_active Expired
- 1972-11-02 OA OA54739A patent/OA04212A/xx unknown
- 1972-11-13 AT AT964472A patent/AT339313B/de not_active IP Right Cessation
- 1972-11-16 IL IL40858A patent/IL40858A/xx unknown
- 1972-11-17 SU SU1855788A patent/SU474985A3/ru active
- 1972-11-30 IE IE1463/72A patent/IE36968B1/xx unknown
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