LU87122A1 - Nouveaux derives de la pilocarpine,leur preparation et leur utilisation comme medicaments - Google Patents

Nouveaux derives de la pilocarpine,leur preparation et leur utilisation comme medicaments Download PDF

Info

Publication number: LU87122A1
Authority: LU; Luxembourg
Prior art keywords: methyl; formula; acid addition; signifies; compound
Prior art date: 1987-01-31

Application number

LU87122A

Other languages

English (en)

French (fr)

Original Assignee

Sandoz Sa

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1987-01-31

Filing date

1988-01-28

Publication date

1988-08-23

1988-01-28 Application filed by Sandoz Sa filed Critical Sandoz Sa

1988-08-23 Publication of LU87122A1 publication Critical patent/LU87122A1/fr

Links

239000003814 drug Substances 0.000 title claims description 8
238000002360 preparation method Methods 0.000 title claims description 5
QCHFTSOMWOSFHM-WPRPVWTQSA-N (+)-Pilocarpine Chemical class C1OC(=O)[C@@H](CC)[C@H]1CC1=CN=CN1C QCHFTSOMWOSFHM-WPRPVWTQSA-N 0.000 title description 6
150000001875 compounds Chemical class 0.000 claims description 58
239000002253 acid Substances 0.000 claims description 15
150000003839 salts Chemical class 0.000 claims description 15
238000000034 method Methods 0.000 claims description 14
239000001257 hydrogen Substances 0.000 claims description 12
229910052739 hydrogen Inorganic materials 0.000 claims description 12
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
239000012458 free base Substances 0.000 claims description 9
125000000217 alkyl group Chemical group 0.000 claims description 8
208000024827 Alzheimer disease Diseases 0.000 claims description 5
208000010412 Glaucoma Diseases 0.000 claims description 4
VKCLPVFDVVKEKU-UHFFFAOYSA-N S=[P] Chemical compound S=[P] VKCLPVFDVVKEKU-UHFFFAOYSA-N 0.000 claims description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 4
206010026749 Mania Diseases 0.000 claims description 3
206010039966 Senile dementia Diseases 0.000 claims description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
206010028417 myasthenia gravis Diseases 0.000 claims description 3
230000008569 process Effects 0.000 claims description 3
208000020016 psychiatric disease Diseases 0.000 claims description 3
201000000980 schizophrenia Diseases 0.000 claims description 3
230000009466 transformation Effects 0.000 claims description 3
201000010099 disease Diseases 0.000 claims description 2
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 2
150000002431 hydrogen Chemical class 0.000 claims description 2
239000008194 pharmaceutical composition Substances 0.000 claims description 2
239000008024 pharmaceutical diluent Substances 0.000 claims description 2
238000011084 recovery Methods 0.000 claims description 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
JEKWFJIPBJGBJT-WCBMZHEXSA-N (3r,4r)-3-ethyl-4-[(3-methylimidazol-4-yl)methyl]thiolan-2-one Chemical compound C1SC(=O)[C@H](CC)[C@H]1CC1=CN=CN1C JEKWFJIPBJGBJT-WCBMZHEXSA-N 0.000 claims 1
JEKWFJIPBJGBJT-WPRPVWTQSA-N (3s,4r)-3-ethyl-4-[(3-methylimidazol-4-yl)methyl]thiolan-2-one Chemical compound C1SC(=O)[C@@H](CC)[C@H]1CC1=CN=CN1C JEKWFJIPBJGBJT-WPRPVWTQSA-N 0.000 claims 1
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 42
239000000203 mixture Substances 0.000 description 26
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 25
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 22
-1 1-methyl-1H-imidazol-5-yl Chemical group 0.000 description 13
230000000694 effects Effects 0.000 description 13
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 10
239000000155 melt Substances 0.000 description 9
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
230000001713 cholinergic effect Effects 0.000 description 7
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 6
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 6
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
OIPILFWXSMYKGL-UHFFFAOYSA-N acetylcholine Chemical compound CC(=O)OCC[N+](C)(C)C OIPILFWXSMYKGL-UHFFFAOYSA-N 0.000 description 6
229960004373 acetylcholine Drugs 0.000 description 6
239000003480 eluent Substances 0.000 description 6
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
239000012074 organic phase Substances 0.000 description 6
230000003518 presynaptic effect Effects 0.000 description 6
239000000047 product Substances 0.000 description 6
239000000741 silica gel Substances 0.000 description 6
229910002027 silica gel Inorganic materials 0.000 description 6
YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 5
229910021529 ammonia Inorganic materials 0.000 description 5
230000001242 postsynaptic effect Effects 0.000 description 5
229910052938 sodium sulfate Inorganic materials 0.000 description 5
235000011152 sodium sulphate Nutrition 0.000 description 5
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 4
WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 4
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
239000003921 oil Substances 0.000 description 4
235000019198 oils Nutrition 0.000 description 4
229930000680 A04AD01 - Scopolamine Natural products 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
STECJAGHUSJQJN-GAUPFVANSA-N Hyoscine Natural products C1([C@H](CO)C(=O)OC2C[C@@H]3N([C@H](C2)[C@@H]2[C@H]3O2)C)=CC=CC=C1 STECJAGHUSJQJN-GAUPFVANSA-N 0.000 description 3
102000014415 Muscarinic acetylcholine receptor Human genes 0.000 description 3
108050003473 Muscarinic acetylcholine receptor Proteins 0.000 description 3
229940121948 Muscarinic receptor antagonist Drugs 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
STECJAGHUSJQJN-UHFFFAOYSA-N N-Methyl-scopolamin Natural products C1C(C2C3O2)N(C)C3CC1OC(=O)C(CO)C1=CC=CC=C1 STECJAGHUSJQJN-UHFFFAOYSA-N 0.000 description 3
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
241000700159 Rattus Species 0.000 description 3
QCHFTSOMWOSFHM-UHFFFAOYSA-N SJ000285536 Natural products C1OC(=O)C(CC)C1CC1=CN=CN1C QCHFTSOMWOSFHM-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000005557 antagonist Substances 0.000 description 3
210000004027 cell Anatomy 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
VZCYOOQTPOCHFL-OWOJBTEDSA-M fumarate(1-) Chemical compound OC(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-M 0.000 description 3
239000003149 muscarinic antagonist Substances 0.000 description 3
230000000144 pharmacologic effect Effects 0.000 description 3
229960001416 pilocarpine Drugs 0.000 description 3
STECJAGHUSJQJN-FWXGHANASA-N scopolamine Chemical compound C1([C@@H](CO)C(=O)O[C@H]2C[C@@H]3N([C@H](C2)[C@@H]2[C@H]3O2)C)=CC=CC=C1 STECJAGHUSJQJN-FWXGHANASA-N 0.000 description 3
229960002646 scopolamine Drugs 0.000 description 3
229910000029 sodium carbonate Inorganic materials 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
YCCVZRIFCRPGSK-WCBMZHEXSA-N (3r,4r)-3-ethyl-4-[(3-methylimidazol-4-yl)methyl]thiolane-2-thione Chemical compound C1SC(=S)[C@H](CC)[C@H]1CC1=CN=CN1C YCCVZRIFCRPGSK-WCBMZHEXSA-N 0.000 description 2
JYWKEVKEKOTYEX-UHFFFAOYSA-N 2,6-dibromo-4-chloroiminocyclohexa-2,5-dien-1-one Chemical compound ClN=C1C=C(Br)C(=O)C(Br)=C1 JYWKEVKEKOTYEX-UHFFFAOYSA-N 0.000 description 2
229940100578 Acetylcholinesterase inhibitor Drugs 0.000 description 2
XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 2
208000003098 Ganglion Cysts Diseases 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
208000005400 Synovial Cyst Diseases 0.000 description 2
239000000556 agonist Substances 0.000 description 2
239000008346 aqueous phase Substances 0.000 description 2
SIPUZPBQZHNSDW-UHFFFAOYSA-N bis(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
238000001816 cooling Methods 0.000 description 2
229940079593 drug Drugs 0.000 description 2
230000005284 excitation Effects 0.000 description 2
230000000971 hippocampal effect Effects 0.000 description 2
210000001320 hippocampus Anatomy 0.000 description 2
230000002401 inhibitory effect Effects 0.000 description 2
CFHGBZLNZZVTAY-UHFFFAOYSA-N lawesson's reagent Chemical compound C1=CC(OC)=CC=C1P1(=S)SP(=S)(C=2C=CC(OC)=CC=2)S1 CFHGBZLNZZVTAY-UHFFFAOYSA-N 0.000 description 2
ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
239000000472 muscarinic agonist Substances 0.000 description 2
210000001640 nerve ending Anatomy 0.000 description 2
239000011541 reaction mixture Substances 0.000 description 2
230000009467 reduction Effects 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
235000017557 sodium bicarbonate Nutrition 0.000 description 2
229930192474 thiophene Natural products 0.000 description 2
239000003981 vehicle Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
PSRPKRDUWXFVQS-KXNXZCPBSA-N (3r,4r)-3-ethyl-4-[(3-methylimidazol-4-yl)methyl]thiolan-2-one;phosphoric acid Chemical compound OP(O)(O)=O.C1SC(=O)[C@H](CC)[C@H]1CC1=CN=CN1C PSRPKRDUWXFVQS-KXNXZCPBSA-N 0.000 description 1
PSRPKRDUWXFVQS-GNAZCLTHSA-N (3s,4r)-3-ethyl-4-[(3-methylimidazol-4-yl)methyl]thiolan-2-one;phosphoric acid Chemical compound OP(O)(O)=O.C1SC(=O)[C@@H](CC)[C@H]1CC1=CN=CN1C PSRPKRDUWXFVQS-GNAZCLTHSA-N 0.000 description 1
BHKAWXZKFKVZLK-UHFFFAOYSA-N 2,3-ditert-butyl-6-methylphenol Chemical compound CC1=CC=C(C(C)(C)C)C(C(C)(C)C)=C1O BHKAWXZKFKVZLK-UHFFFAOYSA-N 0.000 description 1
PXFISGUPSYAFPW-UHFFFAOYSA-N 3-ethyl-3-methyl-4-[(3-methylimidazol-4-yl)methyl]thiolan-2-one Chemical compound C1SC(=O)C(CC)(C)C1CC1=CN=CN1C PXFISGUPSYAFPW-UHFFFAOYSA-N 0.000 description 1
YHIOTRNEAPZWIZ-UHFFFAOYSA-N 4-[(3-methylimidazol-4-yl)methyl]thiolan-2-one Chemical compound CN1C=NC=C1CC1CC(=O)SC1 YHIOTRNEAPZWIZ-UHFFFAOYSA-N 0.000 description 1
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 1
QLIGUFZPUCEOSB-WCBMZHEXSA-N C(C)[C@H]1C(SC[C@@H]1CC1=CN=CN1C)=NO Chemical compound C(C)[C@H]1C(SC[C@@H]1CC1=CN=CN1C)=NO QLIGUFZPUCEOSB-WCBMZHEXSA-N 0.000 description 1
241000700199 Cavia porcellus Species 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
235000014066 European mistletoe Nutrition 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
UQOFGTXDASPNLL-XHNCKOQMSA-N Muscarine Chemical compound C[C@@H]1O[C@H](C[N+](C)(C)C)C[C@H]1O UQOFGTXDASPNLL-XHNCKOQMSA-N 0.000 description 1
238000005481 NMR spectroscopy Methods 0.000 description 1
235000019502 Orange oil Nutrition 0.000 description 1
RSDOPYMFZBJHRL-UHFFFAOYSA-N Oxotremorine Chemical compound O=C1CCCN1CC#CCN1CCCC1 RSDOPYMFZBJHRL-UHFFFAOYSA-N 0.000 description 1
PIJVFDBKTWXHHD-UHFFFAOYSA-N Physostigmine Natural products C12=CC(OC(=O)NC)=CC=C2N(C)C2C1(C)CCN2C PIJVFDBKTWXHHD-UHFFFAOYSA-N 0.000 description 1
235000012300 Rhipsalis cassutha Nutrition 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
241000221012 Viscum Species 0.000 description 1
230000009471 action Effects 0.000 description 1
239000013543 active substance Substances 0.000 description 1
125000005115 alkyl carbamoyl group Chemical group 0.000 description 1
230000008485 antagonism Effects 0.000 description 1
229910052786 argon Inorganic materials 0.000 description 1
239000012300 argon atmosphere Substances 0.000 description 1
238000013475 authorization Methods 0.000 description 1
239000002585 base Substances 0.000 description 1
230000000903 blocking effect Effects 0.000 description 1
210000004556 brain Anatomy 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
230000008602 contraction Effects 0.000 description 1
238000010908 decantation Methods 0.000 description 1
229940043279 diisopropylamine Drugs 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
231100000673 dose–response relationship Toxicity 0.000 description 1
239000003937 drug carrier Substances 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
210000003405 ileum Anatomy 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
230000007774 longterm Effects 0.000 description 1
230000028161 membrane depolarization Effects 0.000 description 1
230000006386 memory function Effects 0.000 description 1
210000003205 muscle Anatomy 0.000 description 1
230000003387 muscular Effects 0.000 description 1
PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 1
210000001577 neostriatum Anatomy 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
239000010502 orange oil Substances 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
125000004043 oxo group Chemical group O=* 0.000 description 1
239000004031 partial agonist Substances 0.000 description 1
229960001697 physostigmine Drugs 0.000 description 1
PIJVFDBKTWXHHD-HIFRSBDPSA-N physostigmine Chemical compound C12=CC(OC(=O)NC)=CC=C2N(C)[C@@H]2[C@@]1(C)CCN2C PIJVFDBKTWXHHD-HIFRSBDPSA-N 0.000 description 1
RNAICSBVACLLGM-GNAZCLTHSA-N pilocarpine hydrochloride Chemical compound Cl.C1OC(=O)[C@@H](CC)[C@H]1CC1=CN=CN1C RNAICSBVACLLGM-GNAZCLTHSA-N 0.000 description 1
239000002244 precipitate Substances 0.000 description 1
238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
210000002763 pyramidal cell Anatomy 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000012262 resinous product Substances 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
229910021653 sulphate ion Inorganic materials 0.000 description 1
229940095064 tartrate Drugs 0.000 description 1
238000002560 therapeutic procedure Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Bioinformatics & Cheminformatics (AREA)
Engineering & Computer Science (AREA)
General Health & Medical Sciences (AREA)
Veterinary Medicine (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
General Chemical & Material Sciences (AREA)
Pharmacology & Pharmacy (AREA)
Life Sciences & Earth Sciences (AREA)
Animal Behavior & Ethology (AREA)
Chemical Kinetics & Catalysis (AREA)
Public Health (AREA)
Medicinal Chemistry (AREA)
Ophthalmology & Optometry (AREA)
Psychiatry (AREA)
Biomedical Technology (AREA)
Neurology (AREA)
Neurosurgery (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Hydrogenated Pyridines (AREA)
Plural Heterocyclic Compounds (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

LU87122A 1987-01-31 1988-01-28 Nouveaux derives de la pilocarpine,leur preparation et leur utilisation comme medicaments LU87122A1 (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE3702940		1987-01-31
DE3702940		1987-01-31

Publications (1)

Publication Number	Publication Date
LU87122A1 true LU87122A1 (fr)	1988-08-23

Family

ID=6319976

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU87122A LU87122A1 (fr)	1987-01-31	1988-01-28	Nouveaux derives de la pilocarpine,leur preparation et leur utilisation comme medicaments

Country Status (27)

Country	Link
US (1)	US4835174A (de)
JP (1)	JPS63201185A (de)
KR (1)	KR880009013A (de)
AT (1)	AT395852B (de)
AU (1)	AU607966B2 (de)
BE (1)	BE1001005A3 (de)
CA (1)	CA1327805C (de)
CH (1)	CH675721A5 (de)
CS (1)	CS411291A3 (de)
DK (1)	DK46288A (de)
ES (1)	ES2008421A6 (de)
FI (1)	FI90080C (de)
FR (1)	FR2610322B1 (de)
GB (1)	GB2200910B (de)
GR (1)	GR880100042A (de)
HU (1)	HU204047B (de)
IE (1)	IE61989B1 (de)
IL (1)	IL85252A (de)
IT (1)	IT1219827B (de)
LU (1)	LU87122A1 (de)
MY (1)	MY102415A (de)
NL (1)	NL8800099A (de)
NZ (1)	NZ223359A (de)
PH (1)	PH24837A (de)
PT (1)	PT86666B (de)
SE (1)	SE466150B (de)
ZA (1)	ZA88665B (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4882343A (en) *	1987-08-28	1989-11-21	G. D. Searle & Co.	Biarylalkylimidazole derivatives as anti-depressants
US5861431A (en) *	1995-06-07	1999-01-19	Iotek, Inc.	Incontinence treatment
MX389626B (es)	2017-11-17	2025-03-20	Cellix Bio Private Ltd	Compuestos de pilocarpina con ácido lipoico para el tratamiento de trastornos oculares.

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2457047A (en) *	1946-02-13	1948-12-21	Monsanto Chemicals	2-(2'-thenyl)-4, 5-dihydroimidazoles and process for making the same
GB1601310A (en) *	1978-05-23	1981-10-28	Lilly Industries Ltd	Aryl hydantoins
JPS56131579A (en) *	1980-03-17	1981-10-15	Kissei Pharmaceut Co Ltd	Novel 1-substituted imidazole derivative
JPS58150566A (ja) *	1982-03-03	1983-09-07	Yoshitomi Pharmaceut Ind Ltd	新規イミダゾ−ル誘導体
DE3228266A1 (de) *	1982-07-29	1984-02-02	A. Nattermann & Cie GmbH, 5000 Köln	Imidazolylalkylthiophene, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische praeparate
DE3329028A1 (de) *	1983-08-11	1985-02-28	Cassella Ag, 6000 Frankfurt	Substituierte (2-amino-2-imidazolin-1-yl)-essigsaeurederivate, verfahren zu ihrer herstellung, ihre verwendung und sie enthaltende pharmazeutische zubereitungen

1988
- 1988-01-18 NL NL8800099A patent/NL8800099A/nl not_active Application Discontinuation
- 1988-01-18 HU HU88177A patent/HU204047B/hu not_active IP Right Cessation
- 1988-01-26 BE BE8800091A patent/BE1001005A3/fr not_active IP Right Cessation
- 1988-01-27 GB GB8801804A patent/GB2200910B/en not_active Expired - Lifetime
- 1988-01-27 FR FR888801019A patent/FR2610322B1/fr not_active Expired - Lifetime
- 1988-01-28 CA CA000557576A patent/CA1327805C/en not_active Expired - Fee Related
- 1988-01-28 LU LU87122A patent/LU87122A1/fr unknown
- 1988-01-28 CH CH307/88A patent/CH675721A5/de not_active IP Right Cessation
- 1988-01-29 FI FI880430A patent/FI90080C/fi not_active IP Right Cessation
- 1988-01-29 JP JP63021136A patent/JPS63201185A/ja active Pending
- 1988-01-29 ZA ZA88665A patent/ZA88665B/xx unknown
- 1988-01-29 US US07/149,812 patent/US4835174A/en not_active Expired - Fee Related
- 1988-01-29 IE IE24488A patent/IE61989B1/en not_active IP Right Cessation
- 1988-01-29 AU AU10960/88A patent/AU607966B2/en not_active Ceased
- 1988-01-29 PH PH36423A patent/PH24837A/en unknown
- 1988-01-29 DK DK046288A patent/DK46288A/da not_active Application Discontinuation
- 1988-01-29 MY MYPI88000081A patent/MY102415A/en unknown
- 1988-01-29 NZ NZ223359A patent/NZ223359A/en unknown
- 1988-01-29 AT AT0018288A patent/AT395852B/de not_active IP Right Cessation
- 1988-01-29 ES ES8800263A patent/ES2008421A6/es not_active Expired
- 1988-01-29 PT PT86666A patent/PT86666B/pt not_active IP Right Cessation
- 1988-01-29 IL IL85252A patent/IL85252A/xx not_active IP Right Cessation
- 1988-01-29 GR GR880100042A patent/GR880100042A/el unknown
- 1988-01-29 SE SE8800293A patent/SE466150B/sv not_active IP Right Cessation
- 1988-01-29 IT IT47578/88A patent/IT1219827B/it active
- 1988-01-30 KR KR1019880000895A patent/KR880009013A/ko not_active Ceased
1991
- 1991-12-27 CS CS914112A patent/CS411291A3/cs unknown

Also Published As

Publication number	Publication date
IL85252A (en)	1992-03-29
DK46288D0 (da)	1988-01-29
IE61989B1 (en)	1994-12-14
CA1327805C (en)	1994-03-15
PH24837A (en)	1990-10-30
FI880430A0 (fi)	1988-01-29
HUT50168A (en)	1989-12-28
FR2610322A1 (fr)	1988-08-05
FI90080B (fi)	1993-09-15
AU1096088A (en)	1988-08-04
CH675721A5 (de)	1990-10-31
GB2200910A (en)	1988-08-17
BE1001005A3 (fr)	1989-06-06
IT1219827B (it)	1990-05-24
FI880430L (fi)	1988-08-01
IE880244L (en)	1988-07-31
SE8800293D0 (sv)	1988-01-29
NL8800099A (nl)	1988-08-16
ATA18288A (de)	1992-08-15
ES2008421A6 (es)	1989-07-16
HU204047B (en)	1991-11-28
CS411291A3 (en)	1992-06-17
PT86666B (pt)	1992-04-30
GB2200910B (en)	1991-01-16
FI90080C (fi)	1993-12-27
US4835174A (en)	1989-05-30
AU607966B2 (en)	1991-03-21
PT86666A (pt)	1988-02-01
JPS63201185A (ja)	1988-08-19
DK46288A (da)	1988-08-01
ZA88665B (en)	1989-09-27
GB8801804D0 (en)	1988-02-24
FR2610322B1 (fr)	1990-02-16
GR880100042A (el)	1988-12-16
KR880009013A (ko)	1988-09-13
MY102415A (en)	1992-06-17
SE8800293L (sv)	1988-08-01
AT395852B (de)	1993-03-25
IT8847578A0 (it)	1988-01-29
IL85252A0 (en)	1988-07-31
SE466150B (sv)	1992-01-07
NZ223359A (en)	1991-03-26

Publication	Publication Date	Title
EP0302788B1 (de)	1992-02-05	2-[Methyl(4-piperidinyl)]-1,2,3,4-tetrahydro-9H-pyrido[3,4-b]indolderivate, ihre Herstellung und therapeutische Verwendung
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EP0351255B1 (de)	1993-10-13	2-[(4-Piperidinyl)methyl]-1,2,3,4-tetrahydroisochinolin-Derivate, ihre Herstellung und ihre therapeutische Verwendung
EP0004494B1 (de)	1982-02-17	1,3-Dihydro-3-(1-(2-(2,3-dihydro-1,4-benzodioxin-2-yl)2-hydroxy-äthyl)piperidin-4-yl)2H-indol-2-on Derivate, Verfahren zu ihrer Herstellung, ihre Verwendung als Arzneimittel und diese enthaltende pharmazeutische Zubereitungen
EP0114850B1 (de)	1988-06-29	Substituierte 2,5-diamino 1,4-diazole, verfahren zu ihrer herstellung, und diese enthaltende farmazeutische zusammenstellungen
EP0479631A1 (de)	1992-04-08	Spiro[4,5]decanderivate, Verfahren zu ihrer Herstellung und diese enthaltende pharmazeutische Zubereitungen
EP0524846A1 (de)	1993-01-27	2-(Piperidin-1-yl)ethanolderivate, ihre Herstellung und ihre Anwendung in der Therapie
FR2602771A1 (fr)	1988-02-19	Nouveaux derives de la benzyl-4 piperazine, leur preparation et les compositions pharmaceutiques qui les contiennent
LU87122A1 (fr)	1988-08-23	Nouveaux derives de la pilocarpine,leur preparation et leur utilisation comme medicaments
EP1828125B1 (de)	2008-04-09	Arylpiperazinderivate und deren verwendung als für den dopamin-d3-rezeptor selektive liganden
EP0099303A2 (de)	1984-01-25	Benzothiopyranopyridinone und ihre Salze, ihre Herstellung und Anwendung als Arzneimittel und diese enthaltende Zubereitungen
FR2618436A1 (fr)	1989-01-27	Derives de piperidine, leur preparation et leur application en therapeutique
FR2672286A1 (fr)	1992-08-07	Derives de 1-(4-chlorophenyl)-2-[4-(phenylmethyl)piperidin-1-yl]ethanol, leur preparation et leur application en therapeutique.
FR2753970A1 (fr)	1998-04-03	Derives de n-(benzothiazol-2-yl) piperidine-1-ethanamine, leur preparation et leur application en therapeutique
EP0638568B1 (de)	1996-10-09	Substituierte Piperazine, ihre Verfahrensherstellung und die enthaltenen pharmazeutischen Zusammenfassungen
EP0117171B1 (de)	1987-07-01	Aminoderivate von in Stellung 6 durch ein heterocyclisch oder ein alicyclisch substituiertes Pyridazin, Verfahren zu deren Herstellung und Heilmittel die sie enthalten
LU86405A1 (fr)	1986-11-05	Derive antipsychotique du benzisothiazole s-oxyde
EP0433167B1 (de)	1994-03-02	Piperidinderivate, Verfahren zur Herstellung sowie diese enthaltende pharmazeutische Präparate
EP1119564B1 (de)	2002-12-18	Aryl-4-fluoro-4-(2-pyridin-2-yl-ethylamino)-methyl]-piperidin-1-yl-methanone derivate als 5-ht1-rezeptor-agonisten
EP0534856B1 (de)	1997-08-27	Thienocyclopentanonoximether, ihre Herstellung und diese enthaltende Arzneimittel
WO2007060027A1 (fr)	2007-05-31	Derives de isoquinoline et benzo[h]isoquinoline, leur preparation et leur utilisation en therapeutique en tant qu’antagonistes du recepteur de l’histamine h3
EP0859775A1 (de)	1998-08-26	3-(benzofuran-5-yl)oxazolidin-2-one-derivate, ihre herstellung und therapeutische verwendung
LU86769A1 (fr)	1987-09-15	Nouvelles quinazolinones tetracycliques,leur preparation et leur utilisation comme medicaments