ES2194783T3 - Procedimiento para la obtencion de 2-cloro-5-clorome-til-1,3-tiazol. - Google Patents
Procedimiento para la obtencion de 2-cloro-5-clorome-til-1,3-tiazol.Info
- Publication number
- ES2194783T3 ES2194783T3 ES00967893T ES00967893T ES2194783T3 ES 2194783 T3 ES2194783 T3 ES 2194783T3 ES 00967893 T ES00967893 T ES 00967893T ES 00967893 T ES00967893 T ES 00967893T ES 2194783 T3 ES2194783 T3 ES 2194783T3
- Authority
- ES
- Spain
- Prior art keywords
- reacting
- formula
- thiourea
- compound
- compounds
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 abstract 9
- 150000001875 compounds Chemical class 0.000 abstract 7
- 239000000460 chlorine Substances 0.000 abstract 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 4
- 229910052801 chlorine Inorganic materials 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- CFXQEHVMCRXUSD-UHFFFAOYSA-N 1,2,3-Trichloropropane Chemical compound ClCC(Cl)CCl CFXQEHVMCRXUSD-UHFFFAOYSA-N 0.000 abstract 2
- IZRKUJREXIKAQM-UHFFFAOYSA-N 2,3-dichloropropanal Chemical compound ClCC(Cl)C=O IZRKUJREXIKAQM-UHFFFAOYSA-N 0.000 abstract 2
- YJZOPBSZDIBXBG-UHFFFAOYSA-N 2-methylthiophene-3-carboxylic acid Chemical compound CC=1SC=CC=1C(O)=O YJZOPBSZDIBXBG-UHFFFAOYSA-N 0.000 abstract 2
- YNNGZCVDIREDDK-UHFFFAOYSA-N aminocarbamodithioic acid Chemical compound NNC(S)=S YNNGZCVDIREDDK-UHFFFAOYSA-N 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 150000002118 epoxides Chemical class 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- UOORRWUZONOOLO-OWOJBTEDSA-N (E)-1,3-dichloropropene Chemical compound ClC\C=C\Cl UOORRWUZONOOLO-OWOJBTEDSA-N 0.000 abstract 1
- OGYGFUAIIOPWQD-UHFFFAOYSA-N 1,3-thiazolidine Chemical compound C1CSCN1 OGYGFUAIIOPWQD-UHFFFAOYSA-N 0.000 abstract 1
- VRMUIVKEHJSADG-UHFFFAOYSA-N 2-chloro-5-(chloromethyl)-1,3-thiazole Chemical compound ClCC1=CN=C(Cl)S1 VRMUIVKEHJSADG-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 150000003840 hydrochlorides Chemical class 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 125000006239 protecting group Chemical group 0.000 abstract 1
- 150000003573 thiols Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C331/00—Derivatives of thiocyanic acid or of isothiocyanic acid
- C07C331/16—Isothiocyanates
- C07C331/18—Isothiocyanates having isothiocyanate groups bound to acyclic carbon atoms
- C07C331/20—Isothiocyanates having isothiocyanate groups bound to acyclic carbon atoms of a saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/38—Nitrogen atoms
- C07D277/40—Unsubstituted amino or imino radicals
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Procedimiento para la obtención de 2-cloro-5- clorometil-1, 3-tiazol, caracterizado porque un compuesto de la fórmula **fórmula** en la que X significa Cl, -OR, -SR o NR2, donde R significa H o un grupo protector adecuado; Y significa H o Cl y Z significa Cl u O, presentando los compuestos de la fórmula (I) como máximo con doble enlace entre C* y Cl o entre Cl y Z, con la condición de que el enlace entre Cl y Z, cuando Z signifique O, sea un doble enlace y cuando Z signifique Cl, sea un enlace sencillo.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT191499A AT409760B (de) | 1999-11-15 | 1999-11-15 | Verfahren zur herstellung von 2-chlor-5-chlormethyl-1,3-thiazol |
| AT462000 | 2000-01-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2194783T3 true ES2194783T3 (es) | 2003-12-01 |
Family
ID=25597158
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES00967893T Expired - Lifetime ES2194783T3 (es) | 1999-11-15 | 2000-10-20 | Procedimiento para la obtencion de 2-cloro-5-clorome-til-1,3-tiazol. |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US6812348B1 (es) |
| EP (1) | EP1230229B1 (es) |
| JP (1) | JP2003523951A (es) |
| AT (1) | ATE241606T1 (es) |
| AU (1) | AU7789300A (es) |
| DE (1) | DE50002398D1 (es) |
| DK (1) | DK1230229T3 (es) |
| ES (1) | ES2194783T3 (es) |
| PT (1) | PT1230229E (es) |
| WO (1) | WO2001036400A1 (es) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4796738B2 (ja) * | 2000-08-10 | 2011-10-19 | バイエル・クロツプサイエンス・アクチエンゲゼルシヤフト | 2−クロロ−5−クロロメチルチアゾールを精製する方法 |
| JP4561068B2 (ja) * | 2003-09-04 | 2010-10-13 | 株式会社クレハ | 2−クロロ−1,3−チアゾール−5−メタノール誘導体、その製造法および農園芸用病害防除剤 |
| CN114716356B (zh) * | 2022-03-10 | 2023-09-26 | 上海应用技术大学 | 一种铑催化合成异硫氰酸酯类化合物的方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5180833A (en) | 1990-03-16 | 1993-01-19 | Takeda Chemical Industries, Ltd. | Process for the preparation of chlorothiazole derivatives |
| GB9518824D0 (en) * | 1995-09-14 | 1995-11-15 | Fine Organics Ltd | Preparation of substituted thiazoles |
| DE19548417A1 (de) * | 1995-12-22 | 1997-06-26 | Bayer Ag | Verfahren zur Herstellung von 2-Chlor-5-chlormethylthiazol |
| IN182219B (es) * | 1996-02-21 | 1999-02-06 | Kuraray Co |
-
2000
- 2000-10-20 US US10/111,011 patent/US6812348B1/en not_active Expired - Fee Related
- 2000-10-20 ES ES00967893T patent/ES2194783T3/es not_active Expired - Lifetime
- 2000-10-20 EP EP00967893A patent/EP1230229B1/de not_active Expired - Lifetime
- 2000-10-20 DE DE50002398T patent/DE50002398D1/de not_active Withdrawn - After Issue
- 2000-10-20 JP JP2001538889A patent/JP2003523951A/ja not_active Withdrawn
- 2000-10-20 PT PT00967893T patent/PT1230229E/pt unknown
- 2000-10-20 AU AU77893/00A patent/AU7789300A/en not_active Abandoned
- 2000-10-20 WO PCT/EP2000/010318 patent/WO2001036400A1/de not_active Ceased
- 2000-10-20 DK DK00967893T patent/DK1230229T3/da active
- 2000-10-20 AT AT00967893T patent/ATE241606T1/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE50002398D1 (de) | 2003-07-03 |
| WO2001036400A1 (de) | 2001-05-25 |
| ATE241606T1 (de) | 2003-06-15 |
| EP1230229B1 (de) | 2003-05-28 |
| AU7789300A (en) | 2001-05-30 |
| PT1230229E (pt) | 2003-08-29 |
| US6812348B1 (en) | 2004-11-02 |
| DK1230229T3 (da) | 2003-09-22 |
| EP1230229A1 (de) | 2002-08-14 |
| JP2003523951A (ja) | 2003-08-12 |
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