Piperidyl derivatives of macrocyclic triazine compounds, possessing a stabilizing activity for polymers, and processes for their preparation

Claim 2

A compound of the formula (I) ##STR39## in which R 1 is hydrogen, C 1 -C 18 -alkyl, C 3 -C 18 -alkenyl, C 5 -C 18 -cycloalkyl, substituted or unsubstituted C 6 -C 18 -aryl, substituted or unsubstituted C 7 -C 18 -aralkyl, an --R 8 --Y radical, in which R 8 is C 2 -C 6 -alkylene and Y is --O--R 9 or ##STR40## R 9 being hydrogen or C 1 -C 18 -alkyl and R 10 and R 11 , which may be identical or different, being C 1 -C 6 -alkyl, 2,2,6,6-tetramethyl-piperid-4-yl or 1,2,2,6,6-pentamethyl-piperid-4-yl, or R 1 is a radical of the formula (II) ##STR41## in which n is zero or 1, r is zero, 1, 2 or 3, R 12 is hydrogen, C 1 -C 12 -alkyl, C 3 -C 12 -alkenyl or -alkynyl, substituted or unsubstituted C 7 -C 12 -aralkyl, C 1 -C 12 -acyl, 2,3-epoxypropyl or ##STR42## in which R 13 is hydrogen, methyl, ethyl or phenyl and R 14 is hydrogen, C 1 -C 12 -alkyl, C 3 -C 12 -alkenyl, C 7 -C 12 -aralkyl or C 1 -C 12 -acyl, or R 1 is a radical of the formula (III) ##STR43## in which R 15 is hydrogen, C 1 -C 8 -alkoxy, C 3 -C 8 -alkenyloxy or benzyloxy and R 13 is as defined above, and X is >O, >S or >N-R 16 , in which R 16 has the same meaning as R 1 , and the radical R 1 --X--, considered as a whole, can also be chlorine or pyrrolidin-1-yl, piperid-1-yl or hexahydroazepin-1-yl, R 2 , R 4 , R 5 and R 7 , which may be identical or different, are hydrogen, C 1 -C 12 -alkyl, C 2 -C 6 -hydroxyalkyl, C 3 -C 12 -alkenyl, C 5 -C 12 -cycloalkyl, substituted or unsubstituted C 6 -C 12 -aryl, substituted or unsubstituted C 7 -C 12 -aralkyl or a radical of the formula (II), and R 3 and R 6 , which may be identical or different, are C 2 -C 12 -alkylene, C 4 -C 12 -iminodialkylene or -oxadialkylene, C 5 -C 12 -cycloalkylene, C 6 -C 12 -arylene or C 7 -C 12 -aralkylene, and at least one of the radicals R 1 , R 2 , R 4 , R 5 and R 7 in formula (I) is a radical of the formula (II).

Claim 3

A compound of the formula (I) according to claim 1, in which R 1 and R 16 , which may be identical or different, are C 1 -C 12 -alkyl, C 3 -C 12 -alkenyl, C 5 -C 12 -cycloalkyl, C 6 -C 12 -aryl, C 7 -C 12 -aralkyl, 2,2,6,6-tetramethyl-piperid-4-yl or 1,2,2,6,6-pentamethyl-piperid-4-yl, R 2 , R 4 , R 5 and R 7 , which may be identical or different, are C 1 -C 4 -alkyl, C 2 -C 3 -hydroxyalkyl, C 3 -C 6 -alkenyl, C 5 -C 8 -cycloalkyl, C 6 -C 8 -aryl, C 7 -C 12 -aralkyl, 2,2,6,6-tetramethyl-piperid-4-yl or 1,2,2,6,6-pentamethyl-piperid-4-yl, R 3 and R 6 , which may be identical or different, are C 2 -C 6 -alkylene, C 4 -C 6 -iminodialkylene or C 4 -C 6 -oxadialkylene, R 8 is C 2 -C 4 -alkylene, R 9 is hydrogen or C 1 -C 12 -alkyl, R 10 and R 11 , which may be identical or different, are C 1 -C 4 -alkyl, 2,2,6,6-tetramethyl-piperid-4-yl or 1,2,2,6,6-pentamethyl-piperid-4-yl, R 12 is hydrogen, C 1 -C 6 -alkyl, C 3 -C 6 -alkenyl or -alkynyl, benzyl, C 1 -C 6 -acyl, 2,3-epoxypropyl or 2-hydroxyethyl, R 13 is hydrogen or methyl, R 14 is hydrogen, C 1 -C 6 -alkyl, C 3 -C 6 -alkenyl, benzyl or C 1 -C 6 -acyl, and R 15 is hydrogen, C 1 -C 6 -alkoxy, allyloxy or benzyloxy, and R 1 --X--, considered as a whole is chlorine, piperid-1-yl or hexahydroazepin-1-yl.

Claim 4

A compound of the formula (I) according to claim 1, in which X is >O or >N-R 16 , R 1 and R 16 , which may be identical or different, are hydrogen, C 2 -C 12 -alkyl, cyclohexyl, 2,2,6,6-tetramethyl-piperid-4-yl or 1,2,2,6,6-pentamethyl-piperid-4-yl, R 2 , R 4 , R 5 and R 7 , which may be identical or different, are hydrogen, 2,2,6,6-tetramethyl-piperid-4-yl or 1,2,2,6,6-pentamethyl-piperid-4-yl, R 3 and R 6 are C 2 -C 6 -alkylene, R 8 is C 2 -C 3 -alkylene, R 10 and R 11 , which may be identical or different, are C 1 -C 4 -alkyl, 2,2,6,6-tetramethyl-piperid-4-yl or 1,2,2,6,6-pentamethyl-piperid-4-yl, R 12 is hydrogen or methyl and R 1 --X--, considered as a whole, is chlorine, piperid-1-yl or hexahydroazepin-1-yl.

Claim 5

A process for the preparation of a compound of the formula (I) ##STR44## in which R 1 is hydrogen, C 1 -C 18 -alkyl, C 3 -C 18 -alkenyl, C 5 -C 18 -cycloalkyl, substituted or unsubstituted C 6 -C 18 -aryl, substituted or unsubstituted C 7 -C 18 -aralkyl, an --R 8 --Y radical, in which R 8 is C 2 -C 6 -alkylene and Y is --O--R 9 or ##STR45## R 9 being hydrogen or C 1 -C 18 -alkyl and R 10 and R 11 , which may be identical or different, being C 1 -C 6 -alkyl, 2,2,6,6-tetramethyl-piperid-4-yl or 1,2,2,6,6-pentamethyl-piperid-4-yl, or R 1 is a radical of the formula (II) ##STR46## in which n is zero or 1, r is zero, 1, 2 or 3, R 12 is hydrogen, C 1 -C 12 -alkyl, C 3 -C 12 -alkenyl or -alkynyl, substituted or unsubstituted C 7 -C 12 -aralkyl, C 1 -C 12 -acyl, 2,3-epoxypropyl or ##STR47## in which R 13 is hydrogen, methyl, ethyl or phenyl and R 14 is hydrogen, C 1 -C 12 -alkyl, C 3 -C 12 -alkenyl, C 7 -C 12 -aralkyl or C 1 -C 12 -acyl, or R 1 is a radical of the formula (III) ##STR48## in which R 15 is hydrogen, C 1 -C 8 -alkoxy, C 3 -C 8 -alkenyloxy or benzyloxy and R 13 is as defined above, and X is >O, >S or >N-R 16 , in which R 16 has the same meaning as R 1 , and the radical R 1 --X--, considered as a whole, can also be chlorine or pyrrolidin-1-yl, piperid-1-yl or hexahydroazepin-1-yl, R 2 , R 4 , R 5 and R 7 , which may be identical or different, are hydrogen, C 1 -C 12 -alkyl, C 2 -C 6 -hydroxyalkyl, C 3 -C 12 -alkenyl, C 5 -C 12 -cycloalkyl, substituted or unsubstituted C 6 -C 12 -aryl, substituted or unsubstituted C 7 -C 12 -aralkyl or a radical of the formula (II), and R 3 and R 6 , which may be identical or different, are C 2 -C 12 -alkylene, C 4 -C 12 -iminodialkylene or -oxadialkylene, C 5 -C 12 -cycloalkylene, C 6 -C 12 -arylene or C 7 -C 12 -aralkylene, and at least one of the radicals R 1 , R 2 , R 4 , R 5 and R 7 in formula (I) is a radical of the formula (II), which comprises reacting cyanuric chloride with a diamine of the formula ##STR49## with a diamine of the formula ##STR50## and with a compound of the formula R 1 -XH, in which R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and X are as defined above, in three successive stages, in the presence of an inert organic solvent and of an organic or inorganic base present in at least the stoichiometric ratio with respect to the HCl formed in the reaction.

Claim 6

A process for the preparation of a compound of the formula (I) ##STR44## in which R 1 is hydrogen, C 1 -C 18 -alkyl, C 3 -C 18 -alkenyl, C 5 -C 18 -cycloalkyl, substituted or unsubstituted C 6 -C 18 -aryl, substituted or unsubstituted C 7 -C 18 -aralkyl, an --R 8 --Y radical, in which R 8 is C 2 -C 6 -alkylene and Y is --O--R 9 or ##STR45## R 9 being hydrogen or C 1 -C 18 -alkyl and R 10 and R 11 , which may be identical or different, being C 1 -C 6 -alkyl, 2,2,6,6-tetramethyl-piperid-4-yl or 1,2,2,6,6-pentamethyl-piperid-4-yl, or R 1 is a radical of the formula (II) ##STR46## in which n is zero or 1, r is zero, 1, 2 or 3, R 12 is hydrogen, C 1 -C 12 -alkyl, C 3 -C 12 -alkenyl or -alkynyl, substituted or unsubstituted C 7 -C 12 -aralkyl, C 1 -C 12 -acyl, 2,3-epoxypropyl or ##STR47## in which R 13 is hydrogen, methyl, ethyl or phenyl and R 14 is hydrogen, C 1 -C 12 -alkyl, C 3 -C 12 -alkenyl, C 7 -C 12 -aralkyl or C 1 -C 12 -acyl, or R 1 is a radical of the formula (III) ##STR48## in which R 15 is hydrogen, C 1 -C 8 -alkoxy, C 3 -C 8 -alkenyloxy or benzyloxy and R 13 is as defined above, and X is >O, >S or >N-R 16 , in which R 16 has the same meaning as R 1 , and the radical R 1 --X--, considered as a whole, can also be chlorine or pyrrolidin-1-yl, piperid-1-yl or hexahydroazepin-1-yl, R 2 , R 4 , R 5 and R 7 , which may be identical or different, are hydrogen, C 1 -C 12 -alkyl, C 2 -C 6 -hydroxyalkyl, C 3 -C 12 -alkenyl, C 5 -C 12 -cycloalkyl, substituted or unsubstituted C 6 -C 12 -aryl, substituted or unsubstituted C 7 -C 12 -aralkyl or a radical of the formula (II), and R 3 and R 6 , which may be identical or different, are C 2 -C 12 -alkylene, C 4 -C 12 -iminodialkylene or -oxadialkylene, C 5 -C 12 -cycloalkylene, C 6 -C 12 -arylene or C 7 -C 12 -aralkylene, and at least one of the radicals R 1 , R 2 , R 4 , R 5 and R 7 in formula (I) is a radical of the formula (II), which comprises reacting cyanuric chloride with a diamine of the formula ##STR49## with a diamine of the formula ##STR50## and with a compound of the formula R 1 -XH, in which R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and X are as defined above, in three successive stages, in the presence of an inert organic solvent and of an organic or inorganic base present in at least the stoichiometric ratio with respect to the HCl formed in the reaction.

Claim 7

A process according to claim 4, wherein the reagents are reacted in accordance with the following succession of stages: ##STR51## in which R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and X are as defined above.

Claim 8

A process according to claim 4, wherein the reagents are reacted in accordance with the following succession of stages: ##STR52## in which R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and X are as defined above.

Claim 9

A process according to any one of claims 4 to 6, wherein the three stages are carried out in one and the same reactor, in a single reaction medium, without isolating the intermediates.

Claim 10

A process according to any one of claims 4 to 6, wherein the individual intermediates of the reaction are isolated and employed in the next stage.

Claim 11

A process according to claim 4, in which the inert organic solvents are chosen from the group comprising acetone, methyl ethyl ketone, ether, dioxane, tetrahydrofuran, benzene, toluene, xylene, trimethylbenzene, ethylbenzene, tetralin, decalin, octane and decane.

Claim 12

A process according to any one of claims 4 to 6, wherein the solvent/reagent ratio in the cyclisation stages (c) and (e) is from 6:1 to 100:1, preferably from 6:1 to 20:1.

Claim 13

A process according to claim 4, wherein the reagents are employed in the stoichiometric ratio.

Claim 14

A process according to either of claims 5 and 6, wherein the stages (a) and (d) are carried out at a temperature of between -30° C. and 30° C., preferably between -10° C. and 20° C.

Claim 15

A process according to either of claims 5 and 6, wherein the stages (b) and (e) are carried out at a temperature of between 30° and 100° C., preferably between 40° and 80° C.

Claim 16

A process according to either of claims 5 and 6, wherein the stages (c) and (f) are carried out at a temperature of between 100° and 200° C., preferably between 120° and 180° C.

Claim 17

A light-stabilised, heat-stabilised and oxidation-stabilised polymer composition comprising a synthetic polymer and one or more stabilisers of the formula (I) in an amount of between 0.01 and 5%, preferably between 0.05 and 1%, by weight relative to the weight of the synthetic polymer.

Claim 18

A light-stabilised, heat-stabilised and oxidation-stabilised polymer composition comprising a synthetic polymer and one or more stabilisers of the formula (I) in an amount of between 0.01 and 5%, preferably between 0.05 and 1%, by weight relative to the weight of the synthetic polymer.

Claim 19

A composition according to claim 15, which in addition to the novel stabiliser of the formula (I) comprises other conventional additives for synthetic polymers.

Claim 20

A composition according to claim 15, wherein the synthetic polymer is polyethylene or polypropylene.

Claim 21

A composition according to claim 15, wherein the synthetic polymer is in the form of a fibre, tape or film.