ES352733A2 - Process for preparing 5-nitroimidazoles - Google Patents
Process for preparing 5-nitroimidazolesInfo
- Publication number
- ES352733A2 ES352733A2 ES352733A ES352733A ES352733A2 ES 352733 A2 ES352733 A2 ES 352733A2 ES 352733 A ES352733 A ES 352733A ES 352733 A ES352733 A ES 352733A ES 352733 A2 ES352733 A2 ES 352733A2
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- formula
- acidic conditions
- oxidizing agent
- acetic
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
- C07D233/91—Nitro radicals
- C07D233/92—Nitro radicals attached in position 4 or 5
- C07D233/94—Nitro radicals attached in position 4 or 5 with hydrocarbon radicals, substituted by oxygen or sulfur atoms, attached to other ring members
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
2 - Alkyl - 5 - nitro - imidazole derivatives of the general formula where R and R1 are C 1-7 alkylene and R2 is C 1-4 alkyl, are prepared by contacting a 2-alkyl-5- nitroimidazole of the formula with at least an equivalent amount of a bromo compound of formula R2-S-R-Br under acidic conditions, and oxidizing the resulting thio intermediate with an oxidizing agent selected from peracids, Cr (VI) oxidants and K 2 MnO 4 , in an inert solvent. The preferred acidic conditions comprise using acetic or formic acid as solvent, but organic solvents containing amounts of mineral acid may also be used. The reaction is preferably carried out at temperatures from 80 to 100 C. The resulting thio derivative is isolated. The preferred oxidizing agent is chromium trioxide in acetic acid.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US68252367A | 1967-11-13 | 1967-11-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
ES352733A2 true ES352733A2 (en) | 1969-09-01 |
Family
ID=24740075
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES352733A Expired ES352733A2 (en) | 1967-11-13 | 1968-04-15 | Process for preparing 5-nitroimidazoles |
Country Status (4)
Country | Link |
---|---|
BR (1) | BR6898309D0 (en) |
ES (1) | ES352733A2 (en) |
GB (1) | GB1209394A (en) |
SE (1) | SE349033B (en) |
-
1968
- 1968-04-11 SE SE499068A patent/SE349033B/xx unknown
- 1968-04-15 BR BR19830968A patent/BR6898309D0/en unknown
- 1968-04-15 ES ES352733A patent/ES352733A2/en not_active Expired
- 1968-11-07 GB GB5289968A patent/GB1209394A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
BR6898309D0 (en) | 1973-05-10 |
GB1209394A (en) | 1970-10-21 |
SE349033B (en) | 1972-09-18 |
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