Radically polymerizable composition comprising a redox initiator system based on dihydropyridines

Patent metadata

Field	Value
Publication number	US-2024099942-A1
Application number	US-202318457781-A
Country	US
Kind code	A1
Filing date	Aug 29, 2023
Priority date	Sep 1, 2022
Publication date	Mar 28, 2024
Grant date	—

Abstract

Radically polymerizable dental material, which includes a catalyst paste and a base paste, wherein the catalyst pastes includes an oxidizing agent, preferably a peroxide or hydroperoxide, a radically polymerizable monomer and/or oligomer with acid group and a polyfunctional radically polymerizable monomer, and the base paste comprises a polyfunctional radically polymerizable monomer without an acid group and a dihydropyridine derivative of Formula (1)

The material has good mechanical properties and does not exhibit a bitter taste.

First claim

1 . A dental material which comprises a catalyst paste and a base paste, wherein the catalyst paste comprises:
(a) at least one polyfunctional radically polymerizable monomer without an acid group, (b) optionally at least one monofunctional radically polymerizable monomer without an acid group, (c) at least a radically polymerizable monomer and/or oligomer with an acid group (d) at least one oxidizing agent; and wherein the base paste comprises: (e) at least one polyfunctional radically polymerizable monomer without an acid group, (f) optionally at least one monofunctional radically polymerizable monomer without an acid group, and (g) at least one dihydropyridine derivative according to Formula (I)

in which
R 1 is a C 6 -C 10 aryl group, which can be unsubstituted or substituted by one or more substituents which are selected from branched or linear C 1 -C 20 alkyl groups, C 6 -C 10 aryl groups, —O—C 1 -C 12 alkoxy groups, —S—C 1 -C 12 sulfide groups, CN, NO 2 , ester groups —C(O)O—R 7 , where R 7 is either a branched or linear C 1 -C 20 alkyl group, a C 6 -C 10 aryl group or a C 7 -C 20 -alkylaryl group, and/or acyl groups —C(O)—R 8 , where R 8 is either a branched or linear C 1 -C 20 alkyl group, a C 6 -C 10 aryl group or a C 7 -C 20 -alkylaryl group;
R 2-6 independently of each other are a hydrogen atom; a branched or linear C 1 -C 20 alkyl group, that can be interrupted by one or more S atoms, O atoms, —C(O)O— groups and/or —C(O)NH— groups, and that can be unsubstituted or substituted by one or more substituents selected from C 1 -C 20 alkyl groups, —O—C 1 -C 12 alkoxy groups and/or ester groups —C(O)O—R 7 , where R 7 is either a branched or linear C 1 -C 20 alkyl group, a C 6 -C 10 aryl group or a C 7 -C 20 -alkylaryl group;
a C 3 -C 16 cycloaliphatic group that can be unsubstituted or substituted by one or more substituents selected from branched or linear C 1 -C 20 alkyl groups, and that can be interrupted by one or more S atoms, O atoms, —C(O)O— groups and/or —C(O)NH— groups; or
a C 7 -C 20 -alkylaryl group that can be interrupted by one or more S atoms, O atoms, —C(O)O— groups and/or —C(O)NH— groups, and/or can be unsubstituted or substituted by one or more substituents selected from branched or linear C 1 -C 20 alkyl groups, C 6 -C 10 aryl groups, branched or linear —O—C 1 -C 12 alkoxy groups, ester groups —C(O)O—R 7 , where R 7 is either a branched or linear C 1 -C 20 alkyl group, a C 6 -C 10 aryl group or a C 7 -C 20 -alkylaryl group, and/or acyl groups —C(O)—R 8 , where R 8 is either a branched or linear C 1 -C 20 alkyl group, a C 6 -C 10 aryl group or a C 7 -C 20 -alkylaryl group;

n is 1, 2, 3 or 4,

and wherein the material comprises at least 50% by weight of polyfunctional radically polymerizable monomers or monomers and oligomers, based on the total amount of radically polymerizable monomers and oligomers.

2 . The composition according to claim 1 , wherein the variables of Formula (I) have the following meanings:
R 1 is a C 6 -C 10 aryl group, which can be unsubstituted or substituted by one or more substituents which is/are selected from C 6 -C 10 aryl groups, —O—C 1 -C 12 alkoxy groups, —O—C 1 -C 12 sulfide groups, CN, NO 2 , ester groups —C(O)O—R 7 , where R 7 is a branched or linear C 1 -C 20 alkyl group, and/or acyl groups —C(O)—R 8 , where R 8 is a branched or linear C 1 -C 20 alkyl group; R 4 , R 6 are each a hydrogen atom; R 2 , R 3 , R 5 independently of each other are each a branched or linear C 1 -C 20 alkyl group that can be interrupted by one or more S atoms, O atoms, —C(O)O— groups and/or —C(O)NH— groups and is not interrupted,
a C 3 -C 16 cycloaliphatic group that is unsubstituted or is substituted by one or more branched or linear C 1 -C 10 alkyl groups that can be interrupted by one or more S atoms, O atoms, —C(O)O— groups and/or —C(O)NH— groups and is not interrupted; or
a C 7 -C 20 -alkylaryl group that can be interrupted by one or more S atoms, O atoms, —C(O)O— groups and/or —C(O)NH— groups and is not interrupted, and/or can be substituted by one or more substituents selected from branched or linear C 1 -C 20 alkyl groups, C 6 -C 10 aryl groups, —O—C 1 -C 12 alkoxy groups, ester groups —C(O)O—R 7 , where R 7 is either a branched or linear C 1 -C 20 alkyl group, a C 6 -C 10 aryl group or a C 7 -C 20 -alkylaryl group, and/or acyl groups —C(O)—R 8 , where R 8 is either a branched or linear C 1 -C 20 alkyl group, a C 6 -C 10 aryl group or a C 7 -C 20 -alkylaryl group, and is not substituted,
n 1.

3 . The composition according to claim 1 , wherein
R 1 is a phenyl group, which is unsubstituted or substituted by one substituent selected from a phenyl group, linear —O—C 1 -C 4 alkoxy groups, preferably —OCH 3 , —O—C 1 -C 4 sulfide groups, preferably —SCH 3 , CN, NO 2 , ester groups —C(O)O—R 7 , where R 7 is a branched or preferably linear C 1 -C 4 alkyl group, preferably methyl or ethyl; R 4 , R 6 are each a hydrogen atom; R 2 , R 3 , R 5 independently of each other are each H, a C 7 -C 10 -alkylaryl group, —CH 2 -Ph or —CH 2 CH 2 -Ph, a linear C 1 -C 6 alkyl group that can be substituted by one —C(O)O—R 7 group, where R 7 is ethyl or methyl, or is unsubstituted, n 1, and wherein the residues R 2 to R 6 have the meanings defined in claim 1 .

4 . The composition according to claim 1 , wherein the at least one oxidizing agent is a peroxide, a hydroperoxide, or a mixture thereof.

5 . The composition according to claim 1 , wherein the at least one polyfunctional monomer (a) and the at least one polyfunctional monomer (e) are selected from a polyfunctional (meth)acrylate comprising bisphenol-A-dimethacrylate, bis-GMA (an addition product of methacrylic acid and bisphenol-A-diglycidyl ether), ethoxy- or propoxylated bisphenol-A-dimethacrylates comprising bisphenol A dimethacrylate SR-348c (Sartomer) with 3 ethoxy groups or 2,2-bis[4-(2-methacryloyloxypropoxy)phenyl]propane, urethanes of 2-(hydroxymethyl)-acrylic acid and diisocyanates comprising 2,2,4-trimethylhexamethylene diisocyanate or isophoronic diisocyanate, UDMA (an addition product of 2-hydroxyethyl methacrylate and 2,2,4-trimethylhexamethylene-1,6-diisocyanate), 2-{[(2-(methacryloyloxy)ethoxy)carbonyl]amino} ethyl methacrylate (V-837), tetramethylxylylene diurethane ethylene glycol di(meth)acrylate and tetramethylxylylene diurethane ethylene glycol di(meth)acrylate, respectively, V380 having the following formula

wherein the R groups are each independently H or CH 3 , di-, tri- or tetraethylene glycol dimethacrylate, trimethylol propanetrimethacrylate, pentaerythritol tetramethacrylate and glycerol di- and trimethacrylate, 1,4-butanediol dimethacrylate, 1,10-decanediol dimethacrylate (D3MA), bis(methacryloyloxymethyl)tricyclo-[5.2.1.02,6]decane (DCP), polyethylene glycol or polypropylene glycol dimethacrylates, comprising polyethylene glycol 200-dimethacrylate or polyethylene glycol 400-dimethacrylate (PEG-200-DMA or PEG-400-DMA) or 1,12-dodecanediol dimethacrylate, and a mixture thereof, Bis-GMA, UDMA, V-380, triethylene glycol dimethacrylate (TEGDMA), PEG-400-DMA (NK ester 9G) or a mixture thereof.

6 . The composition according to claim 1 , wherein the monofunctional monomers (b) and (f) are selected from monofunctional (meth)acrylates comprising benzyl, tetrahydrofurfuryl, isobornyl (meth)acrylate, p-cumylphenoxyethylene glycol methacrylate (CMP-1E), 2-([1,1′-biphenyl]-2-oxy)ethyl methacrylate (PEM=MA-836), tricyclodecane methyl (meth)acrylate, 2-(2-biphenyloxy)ethyl(meth)acrylate and a mixture thereo

Assignees

• Ivoclar Vivadent Ag
• Centre Nat Rech Scient
• Univ Haute Alsace

Inventors

• Fässler Pascal
• Lamparth Iris
• Catel Yohann
• Schnur Thomas
• Lalevée Jacques
• Thetiot Estelle

Classifications

• A61K6/891 Primary

  Compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds · CPC title

• A61K6/61 Primary

  Cationic, anionic or redox initiators · CPC title

• A61K6/62

  Photochemical radical initiators · CPC title

• A61K6/77

  Glass · CPC title

• A61K6/20

  Protective coatings for natural or artificial teeth, e.g. sealings, dye coatings or varnish · CPC title