PL445909A1 - Derivatives 1.1-dimethox-1-fenyl-propan-2-on, methods of producing derivatives 1.1-dimetox-1-fenyl-propan-2-on and use of derivatives 1.1-dimetoxy-1-fenyl-propan-2-on - Google Patents
Derivatives 1.1-dimethox-1-fenyl-propan-2-on, methods of producing derivatives 1.1-dimetox-1-fenyl-propan-2-on and use of derivatives 1.1-dimetoxy-1-fenyl-propan-2-onInfo
- Publication number
- PL445909A1 PL445909A1 PL445909A PL44590923A PL445909A1 PL 445909 A1 PL445909 A1 PL 445909A1 PL 445909 A PL445909 A PL 445909A PL 44590923 A PL44590923 A PL 44590923A PL 445909 A1 PL445909 A1 PL 445909A1
- Authority
- PL
- Poland
- Prior art keywords
- group
- propan
- derivatives
- fenyl
- atom
- Prior art date
Links
- NTPMFTZPWOZVGD-UHFFFAOYSA-N 1,1-dimethoxy-1-phenylpropan-2-one Chemical class COC(OC)(C(C)=O)C1=CC=CC=C1 NTPMFTZPWOZVGD-UHFFFAOYSA-N 0.000 abstract 4
- 229910052799 carbon Inorganic materials 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- -1 2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl Chemical group 0.000 abstract 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 2
- 125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 2
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 abstract 2
- 125000002560 nitrile group Chemical group 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000005936 piperidyl group Chemical group 0.000 abstract 2
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 abstract 1
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 abstract 1
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 abstract 1
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 abstract 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Wynalazek dotyczy pochodnych 1,1-dimetoksy-1-fenylo-propan-2-onu, sposobów wytwarzania pochodnych 1,1-dimetoksy-1-fenylo-propan-2-onu i zastosowania pochodnych 1,1-dimetoksy-1-fenylo-propan-2-onu. Pochodne 1,1-dimetoksy-1-fenylo-propan-2-onu opisane są wzorem ogólnym 1, w którym R oznacza a) grupę o wzorze ogólnym 2, w którym podstawnik R1 jest przyłączony do pierścienia benzenowego w pozycji orto, meta lub para względem atomu węgla, poprzez który ten pierścień połączony jest z atomem węgla wiązania podwójnego znajdującego się poza tym pierścieniem, przy czym podstawnik R1 oznacza atom wodoru, grupę metylową, grupę metoksylową, atom fluoru, atom chloru, atom bromu, grupę dimetyloaminową, grupę dietyloaminową, grupę piperydylową, grupę morfolinową, grupę nitrową, grupę trifluorometylową, grupę metylosulfanylową, grupę nitrylową, b) grupę o wzorze ogólnym 2A, w którym podstawnik R3 oznacza grupę 1-naftylową, grupę 2-naftylową, grupę 2,3-dihydrotieno[3,4-b][1,4]dioksyn-5-ylową, grupę 2-furylową, grupę 3-furylową, grupę 2-tienylową, grupę 3-tienylową, grupę N-etylokarbazol-3-ilową. R2 jest podstawnikiem przyłączonym do pierścienia benzenowego w pozycji orto, meta lub para względem atomu węgla, poprzez który ten pierścień połączony jest z atomem węgla poza tym pierścieniem i R2 oznacza atom wodoru, grupę dietyloaminową, grupę metoksylową, grupę nitrylową, atom chloru, atom bromu, grupę izopropylową, grupę piperydylową, grupę morfolinową.The invention relates to 1,1-dimethoxy-1-phenyl-propan-2-one derivatives, methods of preparing 1,1-dimethoxy-1-phenyl-propan-2-one derivatives and the use of 1,1-dimethoxy-1-phenyl-propan-2-one derivatives. 1,1-Dimethoxy-1-phenyl-propan-2-one derivatives are described by the general formula 1, wherein R denotes a) a group of the general formula 2, wherein the substituent R1 is attached to the benzene ring in the ortho, meta or para position with respect to the carbon atom via which this ring is connected to the carbon atom of a double bond located outside this ring, wherein the substituent R1 denotes a hydrogen atom, a methyl group, a methoxy group, a fluorine atom, a chlorine atom, a bromine atom, a dimethylamino group, a diethylamino group, a piperidyl group, a morpholino group, a nitro group, a trifluoromethyl group, a methylsulfanyl group, a nitrile group, b) a group of the general formula 2A, wherein the substituent R3 denotes a 1-naphthyl group, a 2-naphthyl group, a 2,3-dihydrothieno[3,4-b][1,4]dioxin-5-yl, 2-furyl, 3-furyl, 2-thienyl, 3-thienyl, N-ethylcarbazol-3-yl. R2 is a substituent attached to the benzene ring in the ortho, meta or para position with respect to the carbon atom via which this ring is connected to a carbon atom outside this ring and R2 is a hydrogen atom, a diethylamino group, a methoxy group, a nitrile group, a chlorine atom, a bromine atom, an isopropyl group, a piperidyl group, a morpholino group.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL445909A PL445909A1 (en) | 2023-08-25 | 2023-08-25 | Derivatives 1.1-dimethox-1-fenyl-propan-2-on, methods of producing derivatives 1.1-dimetox-1-fenyl-propan-2-on and use of derivatives 1.1-dimetoxy-1-fenyl-propan-2-on |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL445909A PL445909A1 (en) | 2023-08-25 | 2023-08-25 | Derivatives 1.1-dimethox-1-fenyl-propan-2-on, methods of producing derivatives 1.1-dimetox-1-fenyl-propan-2-on and use of derivatives 1.1-dimetoxy-1-fenyl-propan-2-on |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL445909A1 true PL445909A1 (en) | 2025-03-03 |
Family
ID=94771194
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL445909A PL445909A1 (en) | 2023-08-25 | 2023-08-25 | Derivatives 1.1-dimethox-1-fenyl-propan-2-on, methods of producing derivatives 1.1-dimetox-1-fenyl-propan-2-on and use of derivatives 1.1-dimetoxy-1-fenyl-propan-2-on |
Country Status (1)
| Country | Link |
|---|---|
| PL (1) | PL445909A1 (en) |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005264024A (en) * | 2004-03-19 | 2005-09-29 | Toyo Ink Mfg Co Ltd | Photopolymerization initiator |
| CN109545561A (en) * | 2018-12-18 | 2019-03-29 | 湖北大学 | A kind of light-initiated irreversible gel electrolyte and its preparation method and application |
| US20210271163A1 (en) * | 2018-06-29 | 2021-09-02 | Adeka Corporation | Oxime ester compound and photopolymerization initiator containing same |
-
2023
- 2023-08-25 PL PL445909A patent/PL445909A1/en unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005264024A (en) * | 2004-03-19 | 2005-09-29 | Toyo Ink Mfg Co Ltd | Photopolymerization initiator |
| US20210271163A1 (en) * | 2018-06-29 | 2021-09-02 | Adeka Corporation | Oxime ester compound and photopolymerization initiator containing same |
| CN109545561A (en) * | 2018-12-18 | 2019-03-29 | 湖北大学 | A kind of light-initiated irreversible gel electrolyte and its preparation method and application |
Non-Patent Citations (1)
| Title |
|---|
| ALICJA BALCERAK ET AL: "Polymers 2023, 15(5), 1148, 24.02.2023, https://www.mdpi.com/2073-4360/15/5/1148", LATEST ADVANCES IN HIGHLY EFFICIENT DYE-BASED PHOTOINITIATING SYSTEMS FOR RADICAL POLYMERIZATION * |
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