SI9200169A - Method for producing succinyl-choline-halides - Google Patents
Method for producing succinyl-choline-halides Download PDFInfo
- Publication number
- SI9200169A SI9200169A SI19929200169A SI9200169A SI9200169A SI 9200169 A SI9200169 A SI 9200169A SI 19929200169 A SI19929200169 A SI 19929200169A SI 9200169 A SI9200169 A SI 9200169A SI 9200169 A SI9200169 A SI 9200169A
- Authority
- SI
- Slovenia
- Prior art keywords
- catalyst
- formula
- dimethylaminoethanol
- succinic acid
- process according
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 36
- -1 succinylcholine halide Chemical class 0.000 claims description 30
- 238000000034 method Methods 0.000 claims description 24
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims description 18
- 229960002887 deanol Drugs 0.000 claims description 18
- 239000001384 succinic acid Substances 0.000 claims description 17
- 239000003054 catalyst Substances 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 13
- 229940032712 succinylcholine Drugs 0.000 claims description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 10
- 238000002360 preparation method Methods 0.000 claims description 10
- 239000003513 alkali Substances 0.000 claims description 5
- 150000001408 amides Chemical class 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- 238000004821 distillation Methods 0.000 claims description 4
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 claims description 3
- 150000001298 alcohols Chemical class 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- AFRJJFRNGGLMDW-UHFFFAOYSA-N lithium amide Chemical compound [Li+].[NH2-] AFRJJFRNGGLMDW-UHFFFAOYSA-N 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 2
- 150000007524 organic acids Chemical class 0.000 claims description 2
- 239000007858 starting material Substances 0.000 claims description 2
- 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 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims 1
- 229910052744 lithium Inorganic materials 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- 150000002148 esters Chemical class 0.000 description 10
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- 239000003085 diluting agent Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 5
- AXOIZCJOOAYSMI-UHFFFAOYSA-N succinylcholine Chemical compound C[N+](C)(C)CCOC(=O)CCC(=O)OCC[N+](C)(C)C AXOIZCJOOAYSMI-UHFFFAOYSA-N 0.000 description 5
- 229940120904 succinylcholine chloride Drugs 0.000 description 5
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 4
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 4
- 239000001763 2-hydroxyethyl(trimethyl)azanium Substances 0.000 description 3
- 235000019743 Choline chloride Nutrition 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- SGMZJAMFUVOLNK-UHFFFAOYSA-M choline chloride Chemical compound [Cl-].C[N+](C)(C)CCO SGMZJAMFUVOLNK-UHFFFAOYSA-M 0.000 description 3
- 229960003178 choline chloride Drugs 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000003701 inert diluent Substances 0.000 description 2
- JILPJDVXYVTZDQ-UHFFFAOYSA-N lithium methoxide Chemical compound [Li+].[O-]C JILPJDVXYVTZDQ-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 229940050176 methyl chloride Drugs 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical compound O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- ZFFBIQMNKOJDJE-UHFFFAOYSA-N 2-bromo-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(Br)C(=O)C1=CC=CC=C1 ZFFBIQMNKOJDJE-UHFFFAOYSA-N 0.000 description 1
- MTJGVAJYTOXFJH-UHFFFAOYSA-N 3-aminonaphthalene-1,5-disulfonic acid Chemical compound C1=CC=C(S(O)(=O)=O)C2=CC(N)=CC(S(O)(=O)=O)=C21 MTJGVAJYTOXFJH-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- LDHMZIUMVSRSIK-UHFFFAOYSA-N 4-oxo-4-[2-(trimethylazaniumyl)ethoxy]butanoate;hydrochloride Chemical compound [Cl-].C[N+](C)(C)CCOC(=O)CCC(O)=O LDHMZIUMVSRSIK-UHFFFAOYSA-N 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- MUXOBHXGJLMRAB-UHFFFAOYSA-N Dimethyl succinate Chemical compound COC(=O)CCC(=O)OC MUXOBHXGJLMRAB-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- IRXBNHGNHKNOJI-UHFFFAOYSA-N butanedioyl dichloride Chemical compound ClC(=O)CCC(Cl)=O IRXBNHGNHKNOJI-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- XIXADJRWDQXREU-UHFFFAOYSA-M lithium acetate Chemical compound [Li+].CC([O-])=O XIXADJRWDQXREU-UHFFFAOYSA-M 0.000 description 1
- AZVCGYPLLBEUNV-UHFFFAOYSA-N lithium;ethanolate Chemical compound [Li+].CC[O-] AZVCGYPLLBEUNV-UHFFFAOYSA-N 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000000199 molecular distillation Methods 0.000 description 1
- 229940035363 muscle relaxants Drugs 0.000 description 1
- 239000003158 myorelaxant agent Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- BDAWXSQJJCIFIK-UHFFFAOYSA-N potassium methoxide Chemical compound [K+].[O-]C BDAWXSQJJCIFIK-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- ODZPKZBBUMBTMG-UHFFFAOYSA-N sodium amide Chemical compound [NH2-].[Na+] ODZPKZBBUMBTMG-UHFFFAOYSA-N 0.000 description 1
- 235000011044 succinic acid Nutrition 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/06—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton from hydroxy amines by reactions involving the etherification or esterification of hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C225/00—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
- C07C225/02—Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to acyclic carbon atoms of the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C219/00—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C219/02—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C219/04—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C219/06—Compounds containing amino and esterified hydroxy groups bound to the same carbon skeleton having esterified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having the hydroxy groups esterified by carboxylic acids having the esterifying carboxyl groups bound to hydrogen atoms or to acyclic carbon atoms of an acyclic saturated carbon skeleton
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT0159191A AT396361B (de) | 1991-08-13 | 1991-08-13 | Verfahren zur herstellung von succinylcholinhalogeniden |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SI9200169A true SI9200169A (en) | 1993-03-31 |
Family
ID=3516735
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SI19929200169A SI9200169A (en) | 1991-08-13 | 1992-08-13 | Method for producing succinyl-choline-halides |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US5206420A (es) |
| EP (1) | EP0527364A3 (es) |
| JP (1) | JPH05221939A (es) |
| KR (1) | KR930004247A (es) |
| CN (1) | CN1069485A (es) |
| AR (1) | AR247549A1 (es) |
| AT (1) | AT396361B (es) |
| AU (1) | AU648920B2 (es) |
| BR (1) | BR9203111A (es) |
| CA (1) | CA2072735A1 (es) |
| CZ (1) | CZ249092A3 (es) |
| FI (1) | FI923603A (es) |
| HU (1) | HU210858B (es) |
| IL (1) | IL102231A0 (es) |
| MX (1) | MX9204676A (es) |
| MY (1) | MY153953A (es) |
| NO (1) | NO922801L (es) |
| NZ (1) | NZ243820A (es) |
| PL (1) | PL295591A1 (es) |
| SI (1) | SI9200169A (es) |
| SK (1) | SK249092A3 (es) |
| TW (1) | TW207994B (es) |
| YU (1) | YU65092A (es) |
| ZA (1) | ZA925011B (es) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2002287C (en) * | 1988-11-07 | 2002-03-12 | Thomas L. Brandt | Glass container transparent coating system |
| DE19503279C2 (de) * | 1995-02-02 | 1998-11-12 | Henkel Kgaa | Kation- und/oder Amphooligomere |
| WO2014024207A1 (en) | 2012-08-06 | 2014-02-13 | Neon Laboratories Ltd. | Process for preparation of succinylcholine chloride |
| CN110776435A (zh) * | 2018-07-31 | 2020-02-11 | 上海旭东海普药业有限公司 | 一种氯化琥珀胆碱的制备方法 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE970075C (de) * | 1952-07-05 | 1958-08-21 | Asta Werke Ag Chem Fab | Verfahren zur Herstellung von Bernsteinsaeure-bis-(ª-N-dimethyl- bzw. -diaethylaminoaethylester) |
-
1991
- 1991-08-13 AT AT0159191A patent/AT396361B/de not_active IP Right Cessation
-
1992
- 1992-06-17 IL IL102231A patent/IL102231A0/xx unknown
- 1992-06-24 US US07/903,324 patent/US5206420A/en not_active Expired - Fee Related
- 1992-06-24 YU YU65092A patent/YU65092A/sh unknown
- 1992-06-25 MY MYPI92001077A patent/MY153953A/en unknown
- 1992-06-27 TW TW081105085A patent/TW207994B/zh active
- 1992-06-29 CA CA002072735A patent/CA2072735A1/en not_active Abandoned
- 1992-07-06 ZA ZA925011A patent/ZA925011B/xx unknown
- 1992-07-15 NO NO92922801A patent/NO922801L/no unknown
- 1992-07-17 AR AR92322764A patent/AR247549A1/es active
- 1992-07-18 CN CN92105860A patent/CN1069485A/zh active Pending
- 1992-07-29 AU AU20665/92A patent/AU648920B2/en not_active Ceased
- 1992-08-01 EP EP19920112533 patent/EP0527364A3/de not_active Withdrawn
- 1992-08-03 NZ NZ243820A patent/NZ243820A/en unknown
- 1992-08-11 PL PL29559192A patent/PL295591A1/xx unknown
- 1992-08-11 JP JP4214359A patent/JPH05221939A/ja not_active Withdrawn
- 1992-08-11 KR KR1019920014397A patent/KR930004247A/ko not_active Application Discontinuation
- 1992-08-12 BR BR929203111A patent/BR9203111A/pt not_active Application Discontinuation
- 1992-08-12 HU HU9202622A patent/HU210858B/hu not_active IP Right Cessation
- 1992-08-12 SK SK2490-92A patent/SK249092A3/sk unknown
- 1992-08-12 CZ CS922490A patent/CZ249092A3/cs unknown
- 1992-08-12 FI FI923603A patent/FI923603A/fi not_active Application Discontinuation
- 1992-08-12 MX MX9204676A patent/MX9204676A/es unknown
- 1992-08-13 SI SI19929200169A patent/SI9200169A/sl unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP0527364A3 (en) | 1993-05-05 |
| CA2072735A1 (en) | 1993-02-14 |
| HU9202622D0 (en) | 1992-10-28 |
| YU65092A (sh) | 1994-11-15 |
| CN1069485A (zh) | 1993-03-03 |
| SK249092A3 (en) | 1994-08-10 |
| FI923603A (fi) | 1993-02-14 |
| BR9203111A (pt) | 1993-03-16 |
| ATA159191A (de) | 1992-12-15 |
| AU2066592A (en) | 1993-02-18 |
| KR930004247A (ko) | 1993-03-22 |
| NO922801D0 (no) | 1992-07-15 |
| MX9204676A (es) | 1993-02-01 |
| AT396361B (de) | 1993-08-25 |
| ZA925011B (en) | 1993-04-28 |
| HU210858B (en) | 1995-08-28 |
| CZ249092A3 (en) | 1993-02-17 |
| EP0527364A2 (de) | 1993-02-17 |
| HUT62257A (en) | 1993-04-28 |
| FI923603A0 (fi) | 1992-08-12 |
| NZ243820A (en) | 1993-12-23 |
| US5206420A (en) | 1993-04-27 |
| PL295591A1 (en) | 1993-02-22 |
| TW207994B (es) | 1993-06-21 |
| MY153953A (en) | 2015-04-15 |
| AR247549A1 (es) | 1995-01-31 |
| NO922801L (no) | 1993-02-15 |
| IL102231A0 (en) | 1993-01-14 |
| AU648920B2 (en) | 1994-05-05 |
| JPH05221939A (ja) | 1993-08-31 |
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