FI111630B - Förfarande för framställning av 2-(metyltio)-dinatriumbarbiturat - Google Patents
Förfarande för framställning av 2-(metyltio)-dinatriumbarbiturat Download PDFInfo
- Publication number
- FI111630B FI111630B FI923847A FI923847A FI111630B FI 111630 B FI111630 B FI 111630B FI 923847 A FI923847 A FI 923847A FI 923847 A FI923847 A FI 923847A FI 111630 B FI111630 B FI 111630B
- Authority
- FI
- Finland
- Prior art keywords
- att
- disodium
- vid
- reaction
- methylthio
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 13
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 title claims abstract description 12
- 238000002360 preparation method Methods 0.000 title claims abstract description 12
- 229940125717 barbiturate Drugs 0.000 title claims abstract description 11
- HNYOPLTXPVRDBG-UHFFFAOYSA-N barbituric acid Chemical compound O=C1CC(=O)NC(=O)N1 HNYOPLTXPVRDBG-UHFFFAOYSA-N 0.000 title claims abstract description 11
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 title claims description 12
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims abstract description 22
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 claims abstract description 20
- RGDUXFHSCWTYET-UHFFFAOYSA-N N1C(=S)NC(=O)CC1=O.[Na].[Na] Chemical compound N1C(=S)NC(=O)CC1=O.[Na].[Na] RGDUXFHSCWTYET-UHFFFAOYSA-N 0.000 claims abstract description 12
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229940102396 methyl bromide Drugs 0.000 claims abstract description 10
- BEPAFCGSDWSTEL-UHFFFAOYSA-N dimethyl malonate Chemical compound COC(=O)CC(=O)OC BEPAFCGSDWSTEL-UHFFFAOYSA-N 0.000 claims abstract description 8
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000012467 final product Substances 0.000 claims abstract description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 30
- 238000006243 chemical reaction Methods 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 9
- 239000002798 polar solvent Substances 0.000 claims description 6
- 239000000047 product Substances 0.000 claims description 5
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 4
- 239000002585 base Substances 0.000 claims description 4
- 238000002955 isolation Methods 0.000 claims description 2
- 239000003153 chemical reaction reagent Substances 0.000 claims 2
- RYXPMWYHEBGTRV-UHFFFAOYSA-N Omeprazole sodium Chemical compound [Na+].N=1C2=CC(OC)=CC=C2[N-]C=1S(=O)CC1=NC=C(C)C(OC)=C1C RYXPMWYHEBGTRV-UHFFFAOYSA-N 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- YWOITFUKFOYODT-UHFFFAOYSA-N methanol;sodium Chemical compound [Na].OC YWOITFUKFOYODT-UHFFFAOYSA-N 0.000 claims 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 10
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- 238000001914 filtration Methods 0.000 description 5
- 229960004592 isopropanol Drugs 0.000 description 5
- RIPUYOLXCQRHOZ-UHFFFAOYSA-N 2-methylsulfanyl-1h-pyrimidine-4,6-dione Chemical compound CSC1=NC(=O)CC(=O)N1 RIPUYOLXCQRHOZ-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OYRDHTYPLFMIFN-UHFFFAOYSA-N FC(F)C1C(NC(NC1=O)=S)=O Chemical compound FC(F)C1C(NC(NC1=O)=S)=O OYRDHTYPLFMIFN-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- LHWPSDLHLAAELL-UHFFFAOYSA-N sodium;2-sulfanylidene-1,3-diazinane-4,6-dione Chemical compound [Na].O=C1CC(=O)NC(=S)N1 LHWPSDLHLAAELL-UHFFFAOYSA-N 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 238000009835 boiling Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000003756 stirring Methods 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 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- NBTOZLQBSIZIKS-UHFFFAOYSA-N methoxide Chemical compound [O-]C NBTOZLQBSIZIKS-UHFFFAOYSA-N 0.000 description 1
- 230000011987 methylation Effects 0.000 description 1
- 238000007069 methylation reaction Methods 0.000 description 1
- XTUSEBKMEQERQV-UHFFFAOYSA-N propan-2-ol;hydrate Chemical compound O.CC(C)O XTUSEBKMEQERQV-UHFFFAOYSA-N 0.000 description 1
- OVARTBFNCCXQKS-UHFFFAOYSA-N propan-2-one;hydrate Chemical compound O.CC(C)=O OVARTBFNCCXQKS-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- HLBBKKJFGFRGMU-UHFFFAOYSA-M sodium formate Chemical compound [Na+].[O-]C=O HLBBKKJFGFRGMU-UHFFFAOYSA-M 0.000 description 1
- 235000019254 sodium formate Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F1/00—Compounds containing elements of Groups 1 or 11 of the Periodic Table
- C07F1/04—Sodium compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/60—Three or more oxygen or sulfur atoms
- C07D239/66—Thiobarbituric acids
- C07D239/68—Salts of organic bases; Organic double compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Photoreceptors In Electrophotography (AREA)
- Diaphragms For Electromechanical Transducers (AREA)
- Electroluminescent Light Sources (AREA)
- Cephalosporin Compounds (AREA)
- Detergent Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH255591 | 1991-08-30 | ||
| CH255591 | 1991-08-30 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI923847A0 FI923847A0 (fi) | 1992-08-27 |
| FI923847A FI923847A (fi) | 1993-03-01 |
| FI111630B true FI111630B (sv) | 2003-08-29 |
Family
ID=4236431
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI923847A FI111630B (sv) | 1991-08-30 | 1992-08-27 | Förfarande för framställning av 2-(metyltio)-dinatriumbarbiturat |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US5250689A (sv) |
| EP (1) | EP0529631B1 (sv) |
| JP (1) | JP3218718B2 (sv) |
| KR (1) | KR100242528B1 (sv) |
| AT (1) | ATE172197T1 (sv) |
| AU (1) | AU2203392A (sv) |
| CA (1) | CA2076690C (sv) |
| CZ (1) | CZ281453B6 (sv) |
| DE (1) | DE59209527D1 (sv) |
| ES (1) | ES2124239T3 (sv) |
| FI (1) | FI111630B (sv) |
| HU (1) | HU209834B (sv) |
| IL (1) | IL102986A (sv) |
| SK (1) | SK278681B6 (sv) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE4331223A1 (de) * | 1992-12-24 | 1994-06-30 | Sueddeutsche Kalkstickstoff | Verfahren zur Herstellung von 2-Ethoxy-4,6-dihydroxypyrimidin oder dessen Alkalisalz |
| US5552546A (en) * | 1994-07-28 | 1996-09-03 | Dowelanco | Process for the preparation of 2-ethoxy-4,6-dihydroxypyrimidine |
| CA2208734C (en) * | 1996-07-24 | 2006-05-30 | Lonza Ag | Process for preparing 4,6-bis(difluoro-methoxy)pyrimidine derivatives |
| TWI220428B (en) | 1999-02-05 | 2004-08-21 | Syngenta Participations Ag | Method of producing thiobarbituric acid derivatives |
| MXPA03008121A (es) | 2001-03-15 | 2003-12-12 | Basf Ag | 5-fenilpirimidinas, metodos y productos intermedios para su produccion y uso de las mismas para controlar hongos patogenicos. |
| US20080176744A1 (en) * | 2005-03-10 | 2008-07-24 | Basf Aktiengesellschaft | Use of 4-Aminopyrimidines for Controlling Harmful Fungi, Novel 4-Aminopyrimidines, Processes for Their Preparation and Compositions Comprising Them |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4692524A (en) * | 1986-05-02 | 1987-09-08 | Ciba-Geigy Corporation | Process for the preparation of pyrimidine derivatives |
| DE3925687A1 (de) * | 1989-08-03 | 1991-02-07 | Huels Chemische Werke Ag | Verfahren zur herstellung von 2-(methylthio)barbitursaeure |
| DE3925689A1 (de) * | 1989-08-03 | 1991-02-07 | Huels Chemische Werke Ag | Verfahren zur herstellung von na-thiobarbiturat |
-
1992
- 1992-08-24 CA CA002076690A patent/CA2076690C/en not_active Expired - Lifetime
- 1992-08-26 KR KR1019920015386A patent/KR100242528B1/ko not_active IP Right Cessation
- 1992-08-27 EP EP92114648A patent/EP0529631B1/de not_active Expired - Lifetime
- 1992-08-27 ES ES92114648T patent/ES2124239T3/es not_active Expired - Lifetime
- 1992-08-27 AT AT92114648T patent/ATE172197T1/de active
- 1992-08-27 US US07/936,205 patent/US5250689A/en not_active Expired - Lifetime
- 1992-08-27 DE DE59209527T patent/DE59209527D1/de not_active Expired - Lifetime
- 1992-08-27 JP JP22854092A patent/JP3218718B2/ja not_active Expired - Fee Related
- 1992-08-27 FI FI923847A patent/FI111630B/sv not_active IP Right Cessation
- 1992-08-28 CZ CS922661A patent/CZ281453B6/cs not_active IP Right Cessation
- 1992-08-28 HU HU9202784A patent/HU209834B/hu unknown
- 1992-08-28 IL IL10298692A patent/IL102986A/en not_active IP Right Cessation
- 1992-08-28 SK SK2661-92A patent/SK278681B6/sk not_active IP Right Cessation
- 1992-08-31 AU AU22033/92A patent/AU2203392A/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP0529631A1 (de) | 1993-03-03 |
| ATE172197T1 (de) | 1998-10-15 |
| FI923847A (fi) | 1993-03-01 |
| EP0529631B1 (de) | 1998-10-14 |
| IL102986A (en) | 1996-07-23 |
| DE59209527D1 (de) | 1998-11-19 |
| JP3218718B2 (ja) | 2001-10-15 |
| US5250689A (en) | 1993-10-05 |
| AU2203392A (en) | 1993-03-04 |
| JPH05194425A (ja) | 1993-08-03 |
| CA2076690A1 (en) | 1993-03-01 |
| SK278681B6 (sk) | 1998-01-14 |
| SK266192A3 (en) | 1995-09-13 |
| FI923847A0 (fi) | 1992-08-27 |
| CA2076690C (en) | 2003-01-07 |
| KR930004314A (ko) | 1993-03-22 |
| HU209834B (en) | 1994-11-28 |
| KR100242528B1 (ko) | 2000-03-02 |
| CZ266192A3 (en) | 1993-04-14 |
| CZ281453B6 (cs) | 1996-10-16 |
| ES2124239T3 (es) | 1999-02-01 |
| IL102986A0 (en) | 1993-01-31 |
| HU9202784D0 (en) | 1992-12-28 |
| HUT61986A (en) | 1993-03-29 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| IL24497A (en) | Process for the manufacture of 2,4-diamino-5-benzyl-pyrimidines and novel acetal intermediates obtained thereby | |
| FI111630B (sv) | Förfarande för framställning av 2-(metyltio)-dinatriumbarbiturat | |
| EP0002925A1 (en) | Preparation of herbicidal 2-(4-(pyridyl-2-oxy)-phenoxy)- propionic acid derivatives and compounds thus obtained | |
| US4370280A (en) | Phosphonohydroxyacetonitrile, a process for its preparation and its use as an intermediate product for the preparation of medicaments | |
| JPH04235972A (ja) | アラントインの製造方法 | |
| US5155257A (en) | Process for the preparation of acylaminomethanephosphonic acids | |
| ES2449494T3 (es) | Procedimiento para la producción de ácido 9-cis-retinoico | |
| US4348332A (en) | Phosphonoformaldehyde, a process for its preparation and its use as an intermediate product for the preparation of medicaments | |
| US4275216A (en) | Process for preparing 4(5)-hydroxymethyl 5(4)-lower alkyl imidazoles | |
| US4476306A (en) | Method of preparing 2,4-dihydroxypyrimidine | |
| US2530570A (en) | Pyrimidylmercapto-carboxylic acids | |
| US3412093A (en) | New adenine derivatives and method for their preparation | |
| US3532753A (en) | Pesticidal aromatic amino derivatives of hexahaloacetones | |
| US3929789A (en) | Pyrimidinyl acetic acid derivatives and processes for their production | |
| US5274176A (en) | Process for the production of substituted vinylbenzenes | |
| SU1021341A3 (ru) | Способ получени 2-/2-хлор-4-циклопропилфенил-имино/-имидазолидина или их солей | |
| SU825487A1 (ru) | Способ получения монометилового эфира гидрохинона | |
| KR830002349B1 (ko) | 4-(5)-하이드록시메틸 5(4)-저급알킬이미다졸류의 제조방법 | |
| SU1046240A1 (ru) | Способ получени эфиров @ -алкоксиакриловой или @ -алкоксиметакриловой кислоты | |
| SU887568A1 (ru) | Производные 1-арил-5-карбоксиметилгидантоинов как промежуточные продукты дл синтеза соединений,обладающих рострегулирующими свойствами,и способ их получени | |
| KR810000234B1 (ko) | 벤조 아제핀계 유도체의 제조방법 | |
| SU1413104A1 (ru) | Способ получени 2-метилиндола | |
| HU193454B (en) | Process for producing 3-phenyl-butyraldehyde derivatives | |
| KR950011104B1 (ko) | 불포화 캐톤의 신규한 제조방법 | |
| RU1824401C (ru) | Способ получени 5-метил-2-тиоурацила |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MA | Patent expired |