CH497397A - Verfahren zur Herstellung von Sulfonium- oder Thiouroniumsalzen - Google Patents
Verfahren zur Herstellung von Sulfonium- oder ThiouroniumsalzenInfo
- Publication number
- CH497397A CH497397A CH1247166A CH1247166A CH497397A CH 497397 A CH497397 A CH 497397A CH 1247166 A CH1247166 A CH 1247166A CH 1247166 A CH1247166 A CH 1247166A CH 497397 A CH497397 A CH 497397A
- Authority
- CH
- Switzerland
- Prior art keywords
- formula
- alkyl
- acid
- substituent
- lower alkyl
- Prior art date
Links
- 239000002253 acid Substances 0.000 claims abstract description 11
- 229910052500 inorganic mineral Inorganic materials 0.000 claims abstract description 10
- 239000011707 mineral Substances 0.000 claims abstract description 10
- 238000002360 preparation method Methods 0.000 claims abstract description 8
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 7
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims abstract description 5
- 150000001450 anions Chemical group 0.000 claims abstract description 5
- 125000003118 aryl group Chemical group 0.000 claims abstract description 5
- 125000002877 alkyl aryl group Chemical group 0.000 claims abstract description 4
- 125000002723 alicyclic group Chemical group 0.000 claims abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 21
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 14
- 150000003839 salts Chemical class 0.000 claims description 10
- -1 alkyl sulfide Chemical compound 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 150000007524 organic acids Chemical class 0.000 claims description 9
- 229960000583 acetic acid Drugs 0.000 claims description 8
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 7
- 238000006243 chemical reaction Methods 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 239000012362 glacial acetic acid Substances 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 3
- 239000000543 intermediate Substances 0.000 abstract description 2
- 150000003431 steroids Chemical class 0.000 abstract description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 3
- 239000005977 Ethylene Substances 0.000 abstract 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 abstract 3
- 150000002790 naphthalenes Chemical class 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000005518 carboxamido group Chemical group 0.000 abstract 1
- 239000000262 estrogen Substances 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 18
- QMMFVYPAHWMCMS-UHFFFAOYSA-N Dimethyl sulfide Chemical compound CSC QMMFVYPAHWMCMS-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- 238000001914 filtration Methods 0.000 description 4
- AAMCVENDCXWDPJ-UHFFFAOYSA-N sulfanyl acetate Chemical compound CC(=O)OS AAMCVENDCXWDPJ-UHFFFAOYSA-N 0.000 description 4
- ZNZHGMCIQLVQJP-UHFFFAOYSA-N 1-ethenyl-6-methoxy-3,4-dihydro-2h-naphthalen-1-ol Chemical compound C1CCC(C=C)(O)C=2C1=CC(OC)=CC=2 ZNZHGMCIQLVQJP-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 2
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 2
- 241001342522 Vampyrum spectrum Species 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- LJSQFQKUNVCTIA-UHFFFAOYSA-N diethyl sulfide Chemical compound CCSCC LJSQFQKUNVCTIA-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- JAAJQSRLGAYGKZ-UHFFFAOYSA-N 1,2,3,4-tetrahydronaphthalen-1-ol Chemical group C1=CC=C2C(O)CCCC2=C1 JAAJQSRLGAYGKZ-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 159000000021 acetate salts Chemical class 0.000 description 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 229940106681 chloroacetic acid Drugs 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- GRXPVLPQNMUNNX-MHJRRCNVSA-N estrane Chemical class C1CC2CCCC[C@@H]2[C@@H]2[C@@H]1[C@@H]1CCC[C@@]1(C)CC2 GRXPVLPQNMUNNX-MHJRRCNVSA-N 0.000 description 1
- 230000001076 estrogenic effect Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 229940095574 propionic acid Drugs 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C381/00—Compounds containing carbon and sulfur and having functional groups not covered by groups C07C301/00 - C07C337/00
- C07C381/12—Sulfonium compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C335/00—Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C335/30—Isothioureas
- C07C335/32—Isothioureas having sulfur atoms of isothiourea groups bound to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Steroid Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US48386465A | 1965-08-30 | 1965-08-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH497397A true CH497397A (de) | 1970-10-15 |
Family
ID=23921808
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1247166A CH497397A (de) | 1965-08-30 | 1966-08-29 | Verfahren zur Herstellung von Sulfonium- oder Thiouroniumsalzen |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3501521A (OSRAM) |
| JP (1) | JPS4835067B1 (OSRAM) |
| CH (1) | CH497397A (OSRAM) |
| DE (1) | DE1593078A1 (OSRAM) |
| FR (1) | FR1500986A (OSRAM) |
| GB (1) | GB1153488A (OSRAM) |
| NL (1) | NL6612204A (OSRAM) |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3179638A (en) * | 1960-11-14 | 1965-04-20 | Du Pont | Copolymers prepared from vinyl isothiouronium salts and copolymerizable monoethylenically unsaturated monomers |
| US3318922A (en) * | 1962-10-01 | 1967-05-09 | Merck & Co Inc | 13-substituted alkyl-17-hydroxygona-4-en-3-ones and their 17alpha substitution products |
| GB1080333A (en) * | 1963-11-01 | 1967-08-23 | Takeda Chemical Industries Ltd | New 14-hydroxy steroids |
| US3394151A (en) * | 1965-08-30 | 1968-07-23 | Merck & Co Inc | 1, 3, 5 (10), 8 (14), 9 (11), 15-gonahexaen-17 ones and intermediates obtained in the preparation thereof |
-
1965
- 1965-08-30 US US483864A patent/US3501521A/en not_active Expired - Lifetime
-
1966
- 1966-08-24 GB GB37975/66A patent/GB1153488A/en not_active Expired
- 1966-08-29 DE DE19661593078 patent/DE1593078A1/de active Pending
- 1966-08-29 CH CH1247166A patent/CH497397A/de not_active IP Right Cessation
- 1966-08-29 FR FR74484A patent/FR1500986A/fr not_active Expired
- 1966-08-30 NL NL6612204A patent/NL6612204A/xx unknown
-
1970
- 1970-02-24 JP JP45015328A patent/JPS4835067B1/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| DE1593078A1 (de) | 1970-07-30 |
| FR1500986A (fr) | 1967-11-10 |
| NL6612204A (OSRAM) | 1967-03-01 |
| GB1153488A (en) | 1969-05-29 |
| JPS4835067B1 (OSRAM) | 1973-10-25 |
| US3501521A (en) | 1970-03-17 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE3002678A1 (de) | Verfahren zur herstellung von p-n-alkylbenzoesaeure | |
| EP0572489B1 (de) | Ausgangsverbindungen zur herstellung von calcitriol sowie dessen abkömmlingen, verfahren zur herstellung dieser ausgangsverbindungen sowie zwischenprodukte für dieses verfahren | |
| DE1670681A1 (de) | Verfahren zur Herstellung von 3,1-Benzothiazin-Derivaten | |
| CH497397A (de) | Verfahren zur Herstellung von Sulfonium- oder Thiouroniumsalzen | |
| CH649304A5 (de) | Verfahren zur herstellung von 17beta-hydroxy-3-oxo-17alpha-pregn-4-en-21-carbonsaeure-gamma-lacton und 17beta-hydroxy-3-oxo-17alpha-pregna-4,6-dien-21-carbonsaeure-gamma-lacton. | |
| EP0201452B1 (de) | Verfahren zur Herstellung von 17alpha-Ethinyl-17beta-hydroxy-18-methyl-4,15-estradien-3-on und die neuen Ausgangsverbindungen für dieses Verfahren | |
| DE2631717A1 (de) | Epoxyandrostane und verfahren zu deren herstellung | |
| CH494216A (de) | Verfahren zur Herstellung von in 3-Stellung einer verätherte Hydroxygruppe tragenden 6-Aminomethyl- 3,5-steroiden | |
| DE2617295A1 (de) | Verfahren zur herstellung von spiroverbindungen der steroidreihe | |
| CH456577A (de) | Verfahren zur Herstellung von Dibenzo-cycloheptenen | |
| DE1545825C3 (de) | Verfahren zur Herstellung von 3,5-Dioxo-1,2,4-dithiazolidinen | |
| DE4239945C2 (de) | 14 alpha, 15 alpha-Methylensteroide und Verfahren zu ihrer Herstellung | |
| DE2354327A1 (de) | Verfahren zur herstellung von 6,7benzomorphanen | |
| DE2517770C3 (de) | Verfahren zur Herstellung von | |
| DE914973C (de) | Verfahren zur Herstellung von substituierten threo-konfigurierten ª‡-Halogen-ª‰-oxy-acylamino-aethanen | |
| AT238380B (de) | Verfahren zur Herstellung von 9(11), 16-Pregnadienen | |
| DE1770848A1 (de) | Verfahren zur Herstellung von 3-Methansulfonylphenthiazinen | |
| DE1004173B (de) | Verfahren zur Herstellung von Dodecahydrophenanthren-verbindungen | |
| DE1001679C2 (de) | Verfahren zur Herstellung von 2, 3-Epoxy-12-oxy-(oder keto)- 22-isoallospirostan | |
| DE1130440B (de) | Verfahren zur Herstellung von 2-Aminomethylderivaten von ?-3-Keto-steroiden | |
| DE1238021B (de) | Verfahren zur Herstellung von Verbindungen der Pregnanreihe | |
| DE925475C (de) | Verfahren zur Herstellung von 1-(m-Oxyphenyl)-1-oxo-2-aralkylamino-propanen | |
| AT233184B (de) | Verfahren zur Herstellung von 3-Oxo-Δ<1,4>-steroiden | |
| DE1958533C3 (de) | Verfahren zur Herstellung von 17 alpha-Propadienyl-Gruppen enthaltenden Steroiden | |
| DE2508313C2 (de) | Verfahren zur Herstellung von 17 beta-Hydroxy-4-androsten-3-onen |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |