EP0187702A1
Expired / Lapsed
EP
⏱️ 0.0 years remaining
N-(omega,omega-1-dialkoxy)- and N-(omega,omega-1-dialkenoxy)-alk-1-yl-N,N,N-trisubstituted ammonium surfactants, their preparation and pharmaceutical formulations containing them
Assignee: Syntex USA LLC
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Filing: 1986-01-06
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Granted: —
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Expires: 2006-01-06
Abstract
Abstract This invention relates to compounds of the formula or an optical isomer thereof wherein R' and R 2 are the same or different and are an alkyl or alkenyl group of 6 to 22 carbons; R 3 , R 4 and R 5 are the same or different and are hydrogen, alkyl of 1 to 8 carbon atoms, aryl, aralkyl of 7 to 11 carbons, or when two or three of R 3 , R 4 , and R 5 are taken together to form quinuclidino, piperidino, pyrrolidino, or morpholino; n is 1 to 8; and X is a pharmaceutically acceptable anion.
Inventors
- 👤 Deborah Anne Eppstein
- 👤 Gordon Henry Jones
- 👤 Philips Louis Felgner
- 👤 Richard Bolton Roman
Bibliographic Details
Application Number
—
Jurisdiction
EP
Data Source
google_patents
Last Synchronized
2026-10-23 05:50
CPC Classifications
C; C07; C07D; C07D453/00; C07D453/02; A; A61; A61K; A61K47/00; A61K47/06; A61K47/16; A61K47/18; A61K47/186; A61K9/00; A61K9/0012; A61K9/0014; A61K9/10; A61K9/127; A61K9/1271; A61K9/1272; C12; C12N; C12N15/00; C12N15/09; C12N15/87; C12N15/88
Claims Analysis
Total Claims: 41
Claim 1
Independent Claim
99 words
A compound of the formula or an optical isomer thereof wherein R 1 and R 2 are the same or different and are an alkyl or alkenyl group of 6 to 22 carbons; R 3 , R 4 and R 5 are the same or different and are hydrogen, alkyl of 1 to 8 carbon atoms, aryl, aralkyl of 7 to 11 carbons, or when two or three of R 3 , R 4 , and R 5 are taken together form quinuclidino, pyrrolidino, piperidino, or morpholino; n is 1 to 8; and X is a pharmaceutically acceptable anion.
Claim 2
Dependent Claim
99 words
A compound of the formula or an optical isomer thereof wherein R 1 and R 2 are the same or different and are an alkyl or alkenyl group of 6 to 22 carbons; R 3 , R 4 and R 5 are the same or different and are hydrogen, alkyl of 1 to 8 carbon atoms, aryl, aralkyl of 7 to 11 carbons, or when two or three of R 3 , R 4 , and R 5 are taken together form quinuclidino, pyrrolidino, piperidino, or morpholino; n is 1 to 8; and X is a pharmaceutically acceptable anion.
Claim 3
Dependent Claim
44 words
A compound according to claim 1 wherein R 1 and R 2 are the same and are alkenyl of 10 to 20 carbon atoms, R 3 , R 4 , and R 5 are hydrogen, methyl or ethyl and n is 1 to 4.
Claim 4
Dependent Claim
41 words
A compound according to claim 2 selected from (+) N-(2,3-di-(9-(Z)-octadecenyloxy))-prop-1-yl-N,N-trimethylammonium chloride or an optical isomer thereof; (+) N-(2,3-di-(4-(Z)-decenyloxy))-prop-1-yl-1-trimethylammonium chloride or an optical isomer thereof; (+) N-(3,4-di-(9-(Z)-octadecenyloxy))-but-l-yl-N,N,N-trimethylammonium chloride or an optical isomer thereof; and (+) N-(5,6-di-(9-(Z)-octadecenyloxy))-hex-1-yl-N,N,N-trimethylammonium chloride or an optical isomer thereof.
Claim 5
Dependent Claim
49 words
A compound according to claim 1 wherein R l and R 2 are the same and are alkyl of 10 to 20 carbon atoms, R 3 , R 4 , and R 5 are hydrogen, methyl or ethyl, n is 1 to 4 and X is a halide ion.
Claim 6
Dependent Claim
20 words
A compound according to claim 4 selected from (+) N-(2,3-di-hexadecyloxy)prop-l-yl-N,N,N-trimethylammonium chloride or an optical isomer thereof; and (+) N-(2,3-di-octadecyloxy)prop-1-yl-N,N,N-trimethylammonium chloride.
Claim 7
Dependent Claim
56 words
A compound according to claim I wherein R 1 is' alkyl or alkenyl of 14 to 22 carbon atoms; R 2 is alkyl or alkenyl of 6 to 14 carbon atoms, R 3 , R 4 , and R 5 are hydrogen, methyl or ethyl; n is 1 to 4 and X is a halide ion.
Claim 8
Dependent Claim
20 words
A compound according to claim 6 selected from (+) N-(2-hexadecyloxy-3-decyloxy)-prop-1-yl-N,N,N-trimethylammonium chloride or an optical isomer thereof; and (+) N-(2-hexadecyloxy-3-decyloxy)-prop-1-yl-N,N-dimethylamine hydrochloride.
Claim 9
Dependent Claim
55 words
A liposome formulation which comprises 0.05 to 10% by weight of a drug, 1 to 20% surfactant component by weight of which a compound of formula I of any one of the preceding claims comprises 1 to 100% of this surfactant component, and an aqueous solution in a quantity sufficient to make 100% by volume.
Claim 10
Dependent Claim
56 words
A pharmaceutical formulation which comprises 0.05 to 10% by weight of a drug, 1 to 20% surfactant component by weight of which a compound of formula I of any one of claims 1 to 7 comprises 1 to 100% of this surfactant component, and an aqueous solution in a quantity sufficient to make 100% by volume.
Claim 11
Dependent Claim
29 words
The formulation of claim 9 wherein said drug is 9-(1,3-dihydroxy-2-propoxymethyl)quanine dipalmitate, 6a,9a-difluoro-11β,16α,17α,21-tetrahydroxy-pregna-1,4-diene-3,20-dione-16,17-acetonide (fluocinolone acetonide), 6a,9a-difluoro-11β,16α,17α,21-tetrahydroxy-pregna-1,4-diene-3,20-dione-16,17-acetonide-21-acetate (fluocinonide), 1-[4-(4-chlorophenyl)-2-(2,6-dichlorophenylthio)-n-butyll imidazole nitrate (butaconazole nitrate), beta-interferon, gamma- interferon, 6-0-stearoyl-N-acetylmuramyl-L-a-aminobutyryl-D-isoglutamine or a herpes antigen.
Claim 12
Dependent Claim
27 words
A formulation according to claim 9 or claim 10 wherein said drug comprises 1 to 5% and formula I comprises 50% or more of the surfactant component.
Claim 13
Dependent Claim
60 words
A formulation according to claim 9, 10 or 11 having a compound of formula I wherein R 1 and R 2 are the same and are alkyl or alkenyl of 10 to 20 carbon atoms, R 3 , R 4 , and R 5 are hydrogen, methyl or ethyl, n is 1 to 4 and X is a halide ion.
Claim 14
Dependent Claim
43 words
A formulation according to claim 12 having a compound of formula I which is selected from ( + ) N-(2,3-di-hexadecyloxy)-prop-1-yl-N,N,N-trimethylammonium chloride or an optical isomer thereof; (+) N-(2,3-di-octadecyloxy)-prop-1-yl-N',N,N-trimethylammonium chloride or an optical isomer thereof; and (+) N-t2,3-di-(9-(Z)-octadecenyloxy))-prop-1-yl-N,N,N-trimethylammonium chloride or an optical isomer thereof.
Claim 15
Dependent Claim
62 words
A formulation according to claim 9, 10 or 11 having a compound of formula I wherein R l and R 2 are the same and are alkyl of 10 to 20 carbon atoms, or alkenyl of 10 to 20 carbon atoms and R 3 , R 4 , and R 5 are hydrogen, methyl or ethyl and n is 1 to 4.
Claim 16
Dependent Claim
61 words
A formulation according to claim 9, 10 or 11 wherein R l is alkyl or alkenyl of 14 to 22 carbon atoms and R 2 is a different alkyl group of 6 to 14 carbon atoms; R 3 , R 4 , and R 5 are hydrogen, methyl or ethyl; n is 1 to 4; and X is a halide ion.
Claim 17
Dependent Claim
66 words
A process for the preparation of a compound of any one of claims 1 to 7 which comprises reacting a compound of the formula wherein R 1 and R 2 are as defined above and each R group is defined as R 3 , R 4 , and R 5 are defined above, with an alkyl or aralkyl chloride to form a compound of formula I.
Claim 18
Dependent Claim
186 words
A process for preparation of a compound of the formula or an optical isomer thereof wherein R l and R 2 are the same or different and are an alkyl or alkenyl group of 6 to 22 carbons; none or one of R 3 , R 4 and R 5 is hydrogen, alkyl of 1 to 8 carbon atoms, aryl, or aralkyl of 7 to 11 carbons and two or three of R 3 , R 4 , and R 5 are taken together to form quinuclidino, pyrrolidino, piperidino, or morpholino; n is 1 to 8; and X is a pharmaceutically acceptable anion, which comprises (a) reacting a compound of the formula wherein R 1 and R 2 are as defined above and Y is a halide or p-toluene sulfonyl group with the appropriate hydrocarbon selected from quinuclidine, oyrrolidine, piperidine, or morpholine, optionally followed by (b) reacting the product of step (a) wherein two of R 3 , R 4 , and R 5 are taken together to form pyrrolidino, oiperidino, or morpholino with an alkyl or aralkyl chloride to form a compound of formula I.
Claim 19
Dependent Claim
186 words
A process for preparation of a compound of the formula or an optical isomer thereof wherein R l and R 2 are the same or different and are an alkyl or alkenyl group of 6 to 22 carbons; none or one of R 3 , R 4 and R 5 is hydrogen, alkyl of 1 to 8 carbon atoms, aryl, or aralkyl of 7 to 11 carbons and two or three of R 3 , R 4 , and R 5 are taken together to form quinuclidino, pyrrolidino, piperidino, or morpholino; n is 1 to 8; and X is a pharmaceutically acceptable anion, which comprises (a) reacting a compound of the formula wherein R 1 and R 2 are as defined above and Y is a halide or p-toluene sulfonyl group with the appropriate hydrocarbon selected from quinuclidine, oyrrolidine, piperidine, or morpholine, optionally followed by (b) reacting the product of step (a) wherein two of R 3 , R 4 , and R 5 are taken together to form pyrrolidino, oiperidino, or morpholino with an alkyl or aralkyl chloride to form a compound of formula I.
Claim 20
Dependent Claim
71 words
A compound of the formula or an optical isomer thereof wherein R 1 and R 2 are the same or different and are an alkyl or alkenyl group of 6 to 22 carbons; each R is the same or different and are hydrogen, alkyl of 1 to 8 carbon atoms, aryl, or aralkyl of 7 to 11 carbons or two R groups are taken together to form pyrrolidino, piperidino, or morpholino.
Claim 21
Dependent Claim
71 words
A compound of the formula or an optical isomer thereof wherein R 1 and R 2 are the same or different and are an alkyl or alkenyl group of 6 to 22 carbons; each R is the same or different and are hydrogen, alkyl of 1 to 8 carbon atoms, aryl, or aralkyl of 7 to 11 carbons or two R groups are taken together to form pyrrolidino, piperidino, or morpholino.
Claim 22
Dependent Claim
156 words
A process for the preparation of a compound of the formula or an optical isomer thereof wherein R l and R 2 are the same or different and are an alkyl or alkenyl group of 6 to 22 carbons; R 3 , R 4 and R 5 are the same or different and are hydrogen, alkyl of 1 to 8 carbon atoms, aryl, aralkyl of 7 to 11 carbons or when two or three of R 3 , R 4 , and R 5 are taken together to form quinuclidino, pyrrolidino, piperidino, or morpholino; n is 1 to 8; and X is a pharmaceutically acceptable anion, which comprises reacting a compound of the formula wherein R 1 and R 2 are as defined above and each R group is defined as R 3 , R 4 , and R 5 are defined above, with an alkyl or aralkyl chloride to form a compound of formula I.
Claim 23
Dependent Claim
156 words
A process for the preparation of a compound of the formula or an optical isomer thereof wherein R l and R 2 are the same or different and are an alkyl or alkenyl group of 6 to 22 carbons; R 3 , R 4 and R 5 are the same or different and are hydrogen, alkyl of 1 to 8 carbon atoms, aryl, aralkyl of 7 to 11 carbons or when two or three of R 3 , R 4 , and R 5 are taken together to form quinuclidino, pyrrolidino, piperidino, or morpholino; n is 1 to 8; and X is a pharmaceutically acceptable anion, which comprises reacting a compound of the formula wherein R 1 and R 2 are as defined above and each R group is defined as R 3 , R 4 , and R 5 are defined above, with an alkyl or aralkyl chloride to form a compound of formula I.
Claim 24
Dependent Claim
188 words
A process for preparation of a compound of the formula or an optical isomer thereof wherein R l and R 2 are the same or different and are an alkyl or alkenyl group of 6 to 22 carbons; none or one of R 3 , R 4 and R 5 is hydrogen, alkyl of 1 to 8 carbon atoms, aryl, or aralkyl of 7 to 11 carbons and two or three of R 3 , R 4 , and R 5 are taken together to form quinuclidino, pyrrolidino, piperidino, or morpholino; n is 1 to 8; and X is a pharmaceutically acceptable anion, which comprises (a) reacting a compound of the formula wherein R l and R 2 are as defined above and Y is a halide or p-toluene sulfonyl group with the appropriate hydrocarbon selected from quinuclidine, pyrrolidine, piperidine, or morpholine, optionally followed by (b) reacting the product of step (a) wherein two of R 3 , R 4 , and R 5 are taken together to form pyrrolidino, pi p eridino, or morpholino with an alkyl or aralkyl chloride to form a compound of formula I.
Claim 25
Dependent Claim
188 words
A process for preparation of a compound of the formula or an optical isomer thereof wherein R l and R 2 are the same or different and are an alkyl or alkenyl group of 6 to 22 carbons; none or one of R 3 , R 4 and R 5 is hydrogen, alkyl of 1 to 8 carbon atoms, aryl, or aralkyl of 7 to 11 carbons and two or three of R 3 , R 4 , and R 5 are taken together to form quinuclidino, pyrrolidino, piperidino, or morpholino; n is 1 to 8; and X is a pharmaceutically acceptable anion, which comprises (a) reacting a compound of the formula wherein R l and R 2 are as defined above and Y is a halide or p-toluene sulfonyl group with the appropriate hydrocarbon selected from quinuclidine, pyrrolidine, piperidine, or morpholine, optionally followed by (b) reacting the product of step (a) wherein two of R 3 , R 4 , and R 5 are taken together to form pyrrolidino, pi p eridino, or morpholino with an alkyl or aralkyl chloride to form a compound of formula I.
Claim 26
Dependent Claim
77 words
A process for the preparation of a compound of the formula or an optical isomer thereof wherein R l and R 2 are the same or different and are an alkyl or alkenyl group of 6 to 22 carbons; each R is the same or different and are hydrogen, alkyl of 1 to 8 carbon atoms, aryl, or aralkyl of 7 to 11 carbons or two R groups are taken together to form pyrrolidino, piperidino, or morpholino.
Claim 27
Dependent Claim
77 words
A process for the preparation of a compound of the formula or an optical isomer thereof wherein R l and R 2 are the same or different and are an alkyl or alkenyl group of 6 to 22 carbons; each R is the same or different and are hydrogen, alkyl of 1 to 8 carbon atoms, aryl, or aralkyl of 7 to 11 carbons or two R groups are taken together to form pyrrolidino, piperidino, or morpholino.
Claim 28
Dependent Claim
47 words
A process according to claim 1 or claim 3 wherein R l and R 2 are the same and are alkenyl of 10 to 20 carbon atoms, R 3 , R 4 , and R 5 are hydrogen, methyl or ethyl and n is 1 to 4.
Claim 29
Dependent Claim
45 words
A process according to claim 4 wherein a compound selected from (+) N-(2,3-di-(9-(Z)-octadecenyloxy))-prop-1-yl-N,N-trimethylammonium chloride or an optical isomer thereof; (±) N-(2,3-di-(4-(Z)-decenyloxy)),-prop-1-yl-1-trimethylammonium chloride or an optical isomer thereof; (+) N-(3,4-di-(9-(Z)-octadecenyloxy))-but-l-yl-N,N,N-trimethylammonium chloride or an optical isomer thereof; and (+)N-(5,6-di-(9-(-(Z))-octadecenyloxy))-hex-1-yl-N,N,N-trimethylammonium chloride or an optical isomer thereof, is prepared.
Claim 30
Dependent Claim
52 words
A process according to claim 1 or claim 3 wherein R 1 and R 2 are the same and are alkyl of 10 to 20 carbon atoms, R 3 , R 4 , and R 5 are hydrogen, methyl or ethyl, n is 1 to 4 and X is a halide ion.
Claim 31
Dependent Claim
25 words
A compound according to claim 6 wherein a compound selected from (+) N-(2,3-di-hexadecyloxy)prop-1-yl-N,N,N-trimethylammonium chloride or an optical isomer thereof; and (+) N-(2,3-di-octadecyloxy)prop-1-yl-N,N,N-trimethylammonium chloride is prepared.
Claim 32
Dependent Claim
59 words
A process according to claim 1 or claim 3 wherein R 1 is alkyl or alkenyl of 14 to 22 carbon atoms; R 2 is alkyl or alkenyl of 6 to 14 carbon atoms, R 3 , R 4 , and R 5 are hydrogen, methyl or ethyl; n is 1 to 4 and X is a halide ion.
Claim 33
Dependent Claim
27 words
A process according to claim 8 wherein a compound selected from (+) N-(2-hexadecyloxy-3-decyloxy)-prop-1-yl-N,N,N-tri- . methylammonium chloride or an optical isomer thereof; and (+) N-(2-hexadecyloxy-3-decyloxy)-prop-1-yl-N,N-dimethylamine hydrochloride is prepared.
Claim 34
Dependent Claim
75 words
Use of a compound of formula I as defined in any one of the preceding claims in the manufacture of a liposome formulation which comprises 0.05 to 10% by weight of a drug, 1 to 20% surfactant component by weight of which a compound of formula I of any one of the preceding claims comprises 1 to 100% of this surfactant component, and an aqueous solution in a quantity sufficient to make 100% by volume.
Claim 35
Dependent Claim
77 words
Use of a compound of formula I as defined in any one of claims 1 to 9 in the manufacture of a pharmaceutical formulation which comprises 0.05 to 10% by weight of a drug, 1 to 20% surfactant component by weight of which a compound of formula I of any one of claims 1 to 7 comprises 1 to 100% of this surfactant component, and an aqueous solution in a quantity sufficient to make 100% by volume.
Claim 36
Dependent Claim
30 words
A process according to claim 11 wherein said drug is 9-(1,3-dihydroxy-2-propoxymethyl)quanine dipalmitate, 6a,9a-difluoro-ll6,16a,17a,21-tetrahydroxy-pregna-l,4-diene-3,20-dione-16,17-acetonide (fluocinolone acetonide), 6a,9a-difluoro-11β,16α,17α,21-tetrahydroxy-pregna-1,4-diene-3,20-dione-16,17-acetonide-21-acetate (fluocinonide), 1-[4-(4-chlorophenyl)-2-(2,6-dichlorophenylthio)-n-butyl] imidazole nitrate (butaconazole nitrate), beta-interferon, gamma- interferon, 6-0-stearoyl-N-acetylmuramyl-L-a-aminobutyryl-D-isoglutamine or a herpes antigen.
Claim 37
Dependent Claim
27 words
A process according to claim 11 or claim 12 wherein said drug comprises 1 to 5% and formula I comprises 50% or more of the surfactant component.
Claim 38
Dependent Claim
60 words
A process according to claim 11, 12 or 13 wherein in the compound of formula I, R l and R 2 are the same and are alkyl or alkenyl of 10 to 20 carbon atoms, R 3 , R 4 , and R 5 are hydrogen, methyl or ethyl, n is 1 to 4 and X is a halide ion.
Claim 39
Dependent Claim
40 words
A process according to claim 14 wherein the compound of formula I is selected from (+) N-(2,3-di-hexadecyloxy)-prop-1-yl-N,N,N-trimethylammonium chloride or an optical isomer thereof; (+) N-(2,3-di-octadecyloxy)-prop-1-yl-N,N,N-trimethylammonium chloride or an optical isomer thereof; and (+) N-(2,3-di-(9-(Z)-octadecenyloxy))-prop-1-yl-N,N,N-trimethylammonium chloride or an optical isomer thereof.
Claim 40
Dependent Claim
63 words
A process according to claim 11, 12 or 13 wherein in the compound of formula I R l and R 2 are the same and are alkyl of 10 to 20 carbon atoms, or alkenyl of 10 to 20 , carbon atoms and R 3 , R 4 , and R 5 are hydrogen, methyl or ethyl and n is 1 to 4.
Claim 41
Dependent Claim
67 words
A process according to claim 11, 12 or 13 wherein in the compound of formula I R l is alkyl or alkenyl of 14 to 22 carbon atoms and R 2 is a different alkyl group of 6 to 14 carbon atoms; R 3 , R 4 , and R 5 are hydrogen, methyl or ethyl; n is 1 to 4; and X is a halide ion.
References Cited (Backward Citations)
US3567729A
Cited
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