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Bromo-Directed N-2 Alkylation of NH-1,2,3-Triazoles: Efficient Synthesis of Poly-Substituted 1,2,3-Triazoles
- Source :
- Organic Letters. 11:5490-5493
- Publication Year :
- 2009
- Publisher :
- American Chemical Society (ACS), 2009.
-
Abstract
- Reaction of 4-bromo-NH-1,2,3-triazoles 2 with alkyl halides in the presence of K(2)CO(3) in DMF produced the corresponding 2-substituted 4-bromo-1,2,3-triazoles 5 in a regioselective process. Subsequent Suzuki cross-coupling reaction of these bromides provided an efficient synthesis of 2,4,5-trisubstituted triazoles 3. In addition, reduction of the bromotriazoles by hydrogenation furnished an efficient synthesis of 2,4-disubstituted triazoles 8.
- Subjects :
- chemistry.chemical_classification
Alkylation
Molecular Structure
Chemistry
Organic Chemistry
Halide
Regioselectivity
Stereoisomerism
Triazoles
Biochemistry
Medicinal chemistry
Catalysis
Hydrocarbons, Brominated
Combinatorial Chemistry Techniques
Organic chemistry
Molecule
Physical and Theoretical Chemistry
Alkyl
Subjects
Details
- ISSN :
- 15237052 and 15237060
- Volume :
- 11
- Database :
- OpenAIRE
- Journal :
- Organic Letters
- Accession number :
- edsair.doi.dedup.....7bc6909eccfb887520ba25706d5736f7
- Full Text :
- https://doi.org/10.1021/ol902334x