HU197750B - Process for n-demethylation of morphine alkaloids - Google Patents
Process for n-demethylation of morphine alkaloids Download PDFInfo
- Publication number
- HU197750B HU197750B HU842774A HU277484A HU197750B HU 197750 B HU197750 B HU 197750B HU 842774 A HU842774 A HU 842774A HU 277484 A HU277484 A HU 277484A HU 197750 B HU197750 B HU 197750B
- Authority
- HU
- Hungary
- Prior art keywords
- group
- formula
- hydrogen atom
- carbon atoms
- diphosgene
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 11
- BQJCRHHNABKAKU-KBQPJGBKSA-N morphine Chemical class O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O BQJCRHHNABKAKU-KBQPJGBKSA-N 0.000 title claims description 12
- 229930013053 morphinan alkaloid Natural products 0.000 title claims description 4
- 238000010520 demethylation reaction Methods 0.000 title description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims abstract description 30
- HCUYBXPSSCRKRF-UHFFFAOYSA-N diphosgene Chemical compound ClC(=O)OC(Cl)(Cl)Cl HCUYBXPSSCRKRF-UHFFFAOYSA-N 0.000 claims abstract description 18
- 238000006243 chemical reaction Methods 0.000 claims abstract description 12
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 claims abstract description 11
- 150000001875 compounds Chemical class 0.000 claims abstract description 11
- 239000002253 acid Substances 0.000 claims abstract description 8
- 125000004423 acyloxy group Chemical group 0.000 claims abstract description 7
- 230000007062 hydrolysis Effects 0.000 claims abstract description 6
- 238000006460 hydrolysis reaction Methods 0.000 claims abstract description 6
- 229910052500 inorganic mineral Inorganic materials 0.000 claims abstract description 4
- 238000002955 isolation Methods 0.000 claims abstract description 4
- 239000011707 mineral Substances 0.000 claims abstract description 4
- 238000002360 preparation method Methods 0.000 claims abstract description 4
- 239000002904 solvent Substances 0.000 claims abstract description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 7
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 6
- 229930013930 alkaloid Natural products 0.000 claims description 5
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 3
- 125000001589 carboacyl group Chemical group 0.000 claims description 3
- 235000010755 mineral Nutrition 0.000 claims description 3
- ONBWJWYUHXVEJS-ZTYRTETDSA-N Normorphine Chemical class C([C@@H](NCC1)[C@@H]2C=C[C@@H]3O)C4=CC=C(O)C5=C4[C@@]21[C@H]3O5 ONBWJWYUHXVEJS-ZTYRTETDSA-N 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims 2
- 125000004185 ester group Chemical group 0.000 claims 2
- 150000008282 halocarbons Chemical class 0.000 claims 2
- 150000002576 ketones Chemical class 0.000 claims 2
- 235000015497 potassium bicarbonate Nutrition 0.000 claims 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims 2
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical class [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 claims 1
- 150000007513 acids Chemical class 0.000 claims 1
- 150000003797 alkaloid derivatives Chemical class 0.000 claims 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims 1
- 239000003054 catalyst Substances 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 claims 1
- 239000011736 potassium bicarbonate Substances 0.000 claims 1
- 229910000027 potassium carbonate Inorganic materials 0.000 claims 1
- 235000011181 potassium carbonates Nutrition 0.000 claims 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 abstract description 11
- -1 alkali metal hydrogen carbonates Chemical class 0.000 abstract description 8
- 125000000217 alkyl group Chemical group 0.000 abstract description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 5
- 150000003810 morphinanes Chemical class 0.000 abstract description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 8
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 abstract 5
- 125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 229910000288 alkali metal carbonate Inorganic materials 0.000 abstract 1
- 150000008041 alkali metal carbonates Chemical class 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 238000001816 cooling Methods 0.000 description 9
- 239000000047 product Substances 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- OROGSEYTTFOCAN-DNJOTXNNSA-N codeine Chemical compound C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC OROGSEYTTFOCAN-DNJOTXNNSA-N 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 150000003512 tertiary amines Chemical class 0.000 description 6
- 239000000908 ammonium hydroxide Substances 0.000 description 5
- 238000000605 extraction Methods 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 4
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical compound NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 229960004126 codeine Drugs 0.000 description 4
- OROGSEYTTFOCAN-UHFFFAOYSA-N hydrocodone Natural products C1C(N(CCC234)C)C2C=CC(O)C3OC2=C4C1=CC=C2OC OROGSEYTTFOCAN-UHFFFAOYSA-N 0.000 description 4
- 229910017053 inorganic salt Inorganic materials 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 229960005181 morphine Drugs 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical class OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- PQLFROTZSIMBKR-UHFFFAOYSA-N ethenyl carbonochloridate Chemical compound ClC(=O)OC=C PQLFROTZSIMBKR-UHFFFAOYSA-N 0.000 description 3
- LLPOLZWFYMWNKH-CMKMFDCUSA-N hydrocodone Chemical compound C([C@H]1[C@H](N(CC[C@@]112)C)C3)CC(=O)[C@@H]1OC1=C2C3=CC=C1OC LLPOLZWFYMWNKH-CMKMFDCUSA-N 0.000 description 3
- 229960000240 hydrocodone Drugs 0.000 description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 239000012044 organic layer Substances 0.000 description 3
- 150000003335 secondary amines Chemical class 0.000 description 3
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- IJVCSMSMFSCRME-KBQPJGBKSA-N Dihydromorphine Chemical compound O([C@H]1[C@H](CC[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O IJVCSMSMFSCRME-KBQPJGBKSA-N 0.000 description 2
- OGDVEMNWJVYAJL-LEPYJNQMSA-N Ethyl morphine Chemical compound C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OCC OGDVEMNWJVYAJL-LEPYJNQMSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- OGDVEMNWJVYAJL-UHFFFAOYSA-N Ethylmorphine Natural products C1C(N(CCC234)C)C2C=CC(O)C3OC2=C4C1=CC=C2OCC OGDVEMNWJVYAJL-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- 230000001476 alcoholic effect Effects 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 239000005557 antagonist Substances 0.000 description 2
- 239000012267 brine Substances 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- FZFAMSAMCHXGEF-UHFFFAOYSA-N chloro formate Chemical compound ClOC=O FZFAMSAMCHXGEF-UHFFFAOYSA-N 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 150000001912 cyanamides Chemical class 0.000 description 2
- 239000012649 demethylating agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229960004578 ethylmorphine Drugs 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- TZIHFWKZFHZASV-UHFFFAOYSA-N methyl formate Chemical compound COC=O TZIHFWKZFHZASV-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- INAXVFBXDYWQFN-XHSDSOJGSA-N morphinan Chemical class C1C2=CC=CC=C2[C@]23CCCC[C@H]3[C@@H]1NCC2 INAXVFBXDYWQFN-XHSDSOJGSA-N 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 239000012071 phase Substances 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000005945 von Braun degradation reaction Methods 0.000 description 2
- FQXXSQDCDRQNQE-UHFFFAOYSA-N (-)-thebaine Chemical compound COC1=CC=C2C(N(CC3)C)CC4=CC=C(OC)C5=C4C23C1O5 FQXXSQDCDRQNQE-UHFFFAOYSA-N 0.000 description 1
- JGORUXKMRLIJSV-YNHQPCIGSA-N (4r,4ar,7ar,12bs)-9-methoxy-2,3,4,4a,5,6,7a,13-octahydro-1h-4,12-methanobenzofuro[3,2-e]isoquinoline-7-one Chemical compound O=C([C@@H]1O2)CC[C@H]3[C@H]4CC5=CC=C(OC)C2=C5[C@@]13CCN4 JGORUXKMRLIJSV-YNHQPCIGSA-N 0.000 description 1
- HVQUMOKQAJNIKK-ZTYRTETDSA-N (4r,4ar,7s,7ar,12bs)-1,2,3,4,4a,5,6,7,7a,13-decahydro-4,12-methanobenzofuro[3,2-e]isoquinoline-7,9-diol Chemical compound C([C@@H](NCC1)[C@@H]2CC[C@@H]3O)C4=CC=C(O)C5=C4[C@@]21[C@H]3O5 HVQUMOKQAJNIKK-ZTYRTETDSA-N 0.000 description 1
- IKGNKASQBMZRJL-KOFBORESSA-N (4r,4ar,7s,7ar,12bs)-9-methoxy-1,2,3,4,4a,5,6,7,7a,13-decahydro-4,12-methanobenzofuro[3,2-e]isoquinoline-7-ol Chemical compound O[C@H]([C@@H]1O2)CC[C@H]3[C@H]4CC5=CC=C(OC)C2=C5[C@@]13CCN4 IKGNKASQBMZRJL-KOFBORESSA-N 0.000 description 1
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 description 1
- VXXGFLDAQXZKQE-QLBVAGGCSA-N C(C)OC(=O)N1[C@H]2[C@@H]3CCC([C@H]4[C@@]3(C=3C(=C(C=CC3C2)OC)O4)CC1)=O Chemical compound C(C)OC(=O)N1[C@H]2[C@@H]3CCC([C@H]4[C@@]3(C=3C(=C(C=CC3C2)OC)O4)CC1)=O VXXGFLDAQXZKQE-QLBVAGGCSA-N 0.000 description 1
- PZDCDDVCYJEWCS-YYNKCLGXSA-N ClC(=O)N1[C@H]2[C@@H]3CCC([C@H]4[C@@]3(C=3C(=C(C=CC3C2)OC)O4)CC1)=O Chemical compound ClC(=O)N1[C@H]2[C@@H]3CCC([C@H]4[C@@]3(C=3C(=C(C=CC3C2)OC)O4)CC1)=O PZDCDDVCYJEWCS-YYNKCLGXSA-N 0.000 description 1
- CNEQUQYUPUHQTD-VUICDJBSSA-N ClO.C1=CC(O)=C2C=3[C@@]45[C@@H](O2)C(=O)CC[C@H]4[C@@H](CC13)NCC5 Chemical compound ClO.C1=CC(O)=C2C=3[C@@]45[C@@H](O2)C(=O)CC[C@H]4[C@@H](CC13)NCC5 CNEQUQYUPUHQTD-VUICDJBSSA-N 0.000 description 1
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- 241000557626 Corvus corax Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- SWIRXSKBBSJXGY-UIHHKEIPSA-N Norhydromorphone Chemical compound O=C([C@@H]1O2)CC[C@H]3[C@]4([H])NCC[C@]13C1=C2C(O)=CC=C1C4 SWIRXSKBBSJXGY-UIHHKEIPSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
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- 238000005903 acid hydrolysis reaction Methods 0.000 description 1
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- 239000003153 chemical reaction reagent Substances 0.000 description 1
- RNFNDJAIBTYOQL-UHFFFAOYSA-N chloral hydrate Chemical compound OC(O)C(Cl)(Cl)Cl RNFNDJAIBTYOQL-UHFFFAOYSA-N 0.000 description 1
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- 238000005660 chlorination reaction Methods 0.000 description 1
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- 238000004587 chromatography analysis Methods 0.000 description 1
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- 230000006196 deacetylation Effects 0.000 description 1
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- RBOXVHNMENFORY-DNJOTXNNSA-N dihydrocodeine Chemical compound C([C@H]1[C@H](N(CC[C@@]112)C)C3)C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC RBOXVHNMENFORY-DNJOTXNNSA-N 0.000 description 1
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- XYYVYLMBEZUESM-UHFFFAOYSA-N dihydrocodeine Natural products C1C(N(CCC234)C)C2C=CC(=O)C3OC2=C4C1=CC=C2OC XYYVYLMBEZUESM-UHFFFAOYSA-N 0.000 description 1
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- HNPDNOZNULJJDL-UHFFFAOYSA-N ethyl n-ethenylcarbamate Chemical class CCOC(=O)NC=C HNPDNOZNULJJDL-UHFFFAOYSA-N 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
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- 238000000752 ionisation method Methods 0.000 description 1
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- 231100001231 less toxic Toxicity 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
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- 230000008018 melting Effects 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- 239000003887 narcotic antagonist Substances 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
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- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
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- XLRPYZSEQKXZAA-OCAPTIKFSA-N tropane Chemical compound C1CC[C@H]2CC[C@@H]1N2C XLRPYZSEQKXZAA-OCAPTIKFSA-N 0.000 description 1
- 229930004006 tropane Natural products 0.000 description 1
- 229930004668 tropane alkaloid Natural products 0.000 description 1
- 150000003813 tropane derivatives Chemical class 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- 231100000925 very toxic Toxicity 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D489/00—Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula:
- C07D489/02—Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula: with oxygen atoms attached in positions 3 and 6, e.g. morphine, morphinone
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D489/00—Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula:
- C07D489/06—Heterocyclic compounds containing 4aH-8, 9 c- Iminoethano-phenanthro [4, 5-b, c, d] furan ring systems, e.g. derivatives of [4, 5-epoxy]-morphinan of the formula: with a hetero atom directly attached in position 14
- C07D489/08—Oxygen atom
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Ultra Sonic Daignosis Equipment (AREA)
- Measurement And Recording Of Electrical Phenomena And Electrical Characteristics Of The Living Body (AREA)
- Finger-Pressure Massage (AREA)
- Stringed Musical Instruments (AREA)
- Electrophonic Musical Instruments (AREA)
- Polyesters Or Polycarbonates (AREA)
- Materials For Photolithography (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Other Investigation Or Analysis Of Materials By Electrical Means (AREA)
- Cephalosporin Compounds (AREA)
Priority Applications (19)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU842774A HU197750B (en) | 1984-07-17 | 1984-07-17 | Process for n-demethylation of morphine alkaloids |
| IL75509A IL75509A0 (en) | 1984-07-17 | 1985-06-13 | Process for n-demethylation of morphinane alkaloids |
| IN476/DEL/85A IN166255B (OSRAM) | 1984-07-17 | 1985-06-14 | |
| ES544385A ES8603716A1 (es) | 1984-07-17 | 1985-06-20 | Procedimiento de preparar compuestos de la estructura del n-desmetilmorfinano |
| EP85107895A EP0168686B1 (de) | 1984-07-17 | 1985-06-26 | Verfahren zum N-demethylieren von Morphinan-alkaloiden |
| AT85107895T ATE41933T1 (de) | 1984-07-17 | 1985-06-26 | Verfahren zum n-demethylieren von morphinanalkaloiden. |
| DE8585107895T DE3569244D1 (en) | 1984-07-17 | 1985-06-26 | Process for n-demethylating morphinane alkaloids |
| DD85278546A DD235639A5 (de) | 1984-07-17 | 1985-07-12 | Verfahren zum n-demethylieren von morphinan-alkaloiden |
| PL25455285A PL254552A1 (en) | 1984-07-17 | 1985-07-15 | Method of obtaining derivatives of morphinanoic alcaloides |
| RO119568A RO91516B (ro) | 1984-07-17 | 1985-07-15 | Procedeu pentru prepararea unor derivati de n-demetil-morfinan |
| BG071084A BG44029A3 (en) | 1984-07-17 | 1985-07-15 | Method for preparing of n- dimethyl morphinanic derivatives |
| DK322385A DK322385A (da) | 1984-07-17 | 1985-07-15 | Fremgangsmaade til fremstilling af alkaloider |
| FI852779A FI81583C (fi) | 1984-07-17 | 1985-07-15 | Foerfarande foer n-demetylering av morfinanalkaloider. |
| NO852838A NO161915C (no) | 1984-07-17 | 1985-07-16 | Fremgangsmaate for n-demethylering av morfinan-alkaloider. |
| SU853923700A SU1398776A3 (ru) | 1984-07-17 | 1985-07-16 | Способ получени производных N-деметил-морфинов |
| CS855280A CS251792B2 (en) | 1984-07-17 | 1985-07-16 | Method of compouns preparation with n-demethylmorphinane skeleton |
| JP60156846A JPS6193184A (ja) | 1984-07-17 | 1985-07-16 | Ｎ−脱メチル−モルフイナンアルカロイドの製造方法 |
| YU1174/85A YU45264B (en) | 1984-07-17 | 1985-07-17 | Process for n-demethy morphinanic alkaloids obtaining |
| IL78503A IL78503A (en) | 1984-07-17 | 1986-04-15 | Preparation of(4,5-epoxy)morphinan-6-one hydrazones and semi(thio)carbazones |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU842774A HU197750B (en) | 1984-07-17 | 1984-07-17 | Process for n-demethylation of morphine alkaloids |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| HUT38645A HUT38645A (en) | 1986-06-30 |
| HU197750B true HU197750B (en) | 1989-05-29 |
Family
ID=10961043
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU842774A HU197750B (en) | 1984-07-17 | 1984-07-17 | Process for n-demethylation of morphine alkaloids |
Country Status (18)
| Country | Link |
|---|---|
| EP (1) | EP0168686B1 (OSRAM) |
| JP (1) | JPS6193184A (OSRAM) |
| AT (1) | ATE41933T1 (OSRAM) |
| BG (1) | BG44029A3 (OSRAM) |
| CS (1) | CS251792B2 (OSRAM) |
| DD (1) | DD235639A5 (OSRAM) |
| DE (1) | DE3569244D1 (OSRAM) |
| DK (1) | DK322385A (OSRAM) |
| ES (1) | ES8603716A1 (OSRAM) |
| FI (1) | FI81583C (OSRAM) |
| HU (1) | HU197750B (OSRAM) |
| IL (2) | IL75509A0 (OSRAM) |
| IN (1) | IN166255B (OSRAM) |
| NO (1) | NO161915C (OSRAM) |
| PL (1) | PL254552A1 (OSRAM) |
| RO (1) | RO91516B (OSRAM) |
| SU (1) | SU1398776A3 (OSRAM) |
| YU (1) | YU45264B (OSRAM) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101896463B (zh) * | 2007-12-17 | 2016-08-24 | 马林克罗特有限公司 | 制备(+)阿片类的方法和化合物 |
| EP2222643B1 (en) * | 2007-12-17 | 2019-03-20 | SpecGx LLC | Sinomenine derivatives and processes for their synthesis |
| DE112010001980T8 (de) * | 2009-05-12 | 2012-11-08 | Board Of Regents, The University Of Texas System | Synthese von Morphin und verwandten Derivaten |
| PL2593095T3 (pl) * | 2010-07-16 | 2019-12-31 | Mallinckrodt Llc | (+)-morfinany jako antagoniści receptora toll-podobnego 9 i ich terapeutyczne zastosowania |
| PL2753622T3 (pl) | 2011-09-08 | 2016-07-29 | SpecGx LLC | Wytwarzanie alkaloidów bez oddzielania związków pośrednich |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA948198A (en) * | 1967-08-04 | 1974-05-28 | Gerhard Walther | Production of cyclic amino compounds |
| DE2254298A1 (de) * | 1972-11-06 | 1974-05-16 | Boehringer Sohn Ingelheim | Neue (heteroarylmethyl)-normorphine, deren saeureadditionssalze, verfahren zu deren herstellung sowie deren verwendung als arzneimittel |
| DE2727805A1 (de) * | 1977-06-21 | 1979-01-04 | Goedecke Ag | Verfahren zur herstellung von oxynormorphon |
-
1984
- 1984-07-17 HU HU842774A patent/HU197750B/hu not_active IP Right Cessation
-
1985
- 1985-06-13 IL IL75509A patent/IL75509A0/xx not_active IP Right Cessation
- 1985-06-14 IN IN476/DEL/85A patent/IN166255B/en unknown
- 1985-06-20 ES ES544385A patent/ES8603716A1/es not_active Expired
- 1985-06-26 AT AT85107895T patent/ATE41933T1/de not_active IP Right Cessation
- 1985-06-26 EP EP85107895A patent/EP0168686B1/de not_active Expired
- 1985-06-26 DE DE8585107895T patent/DE3569244D1/de not_active Expired
- 1985-07-12 DD DD85278546A patent/DD235639A5/de not_active IP Right Cessation
- 1985-07-15 FI FI852779A patent/FI81583C/fi not_active IP Right Cessation
- 1985-07-15 PL PL25455285A patent/PL254552A1/xx unknown
- 1985-07-15 RO RO119568A patent/RO91516B/ro unknown
- 1985-07-15 BG BG071084A patent/BG44029A3/xx unknown
- 1985-07-15 DK DK322385A patent/DK322385A/da not_active Application Discontinuation
- 1985-07-16 JP JP60156846A patent/JPS6193184A/ja active Pending
- 1985-07-16 CS CS855280A patent/CS251792B2/cs unknown
- 1985-07-16 NO NO852838A patent/NO161915C/no unknown
- 1985-07-16 SU SU853923700A patent/SU1398776A3/ru active
- 1985-07-17 YU YU1174/85A patent/YU45264B/xx unknown
-
1986
- 1986-04-15 IL IL78503A patent/IL78503A/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| FI81583C (fi) | 1990-11-12 |
| CS251792B2 (en) | 1987-08-13 |
| HUT38645A (en) | 1986-06-30 |
| DD235639A5 (de) | 1986-05-14 |
| YU117485A (en) | 1988-04-30 |
| RO91516A (ro) | 1987-06-30 |
| EP0168686B1 (de) | 1989-04-05 |
| IL78503A (en) | 1990-01-18 |
| SU1398776A3 (ru) | 1988-06-15 |
| DK322385D0 (da) | 1985-07-15 |
| FI852779L (fi) | 1986-01-18 |
| ES8603716A1 (es) | 1986-01-16 |
| DE3569244D1 (en) | 1989-05-11 |
| YU45264B (en) | 1992-05-28 |
| IN166255B (OSRAM) | 1990-03-31 |
| IL75509A0 (en) | 1985-10-31 |
| FI81583B (fi) | 1990-07-31 |
| FI852779A0 (fi) | 1985-07-15 |
| EP0168686A1 (de) | 1986-01-22 |
| PL254552A1 (en) | 1986-07-15 |
| NO161915B (no) | 1989-07-03 |
| JPS6193184A (ja) | 1986-05-12 |
| DK322385A (da) | 1986-01-18 |
| ES544385A0 (es) | 1986-01-16 |
| NO852838L (no) | 1986-01-20 |
| BG44029A3 (en) | 1988-09-15 |
| CS528085A2 (en) | 1986-12-18 |
| NO161915C (no) | 1989-10-11 |
| RO91516B (ro) | 1987-07-01 |
| ATE41933T1 (de) | 1989-04-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| HU90 | Patent valid on 900628 | ||
| HMM4 | Cancellation of final prot. due to non-payment of fee |