Syntheses of 4- and 6-substituted thiazolo[4,5-c]pyridines
β Scribed by Yuhua Huang; Frank Bennett; Vinay Girijavallabhan; Carmen Alvarez; Tze-Ming Chan; Rebecca Osterman; Mary Senior; Cecil Kwong; Namita Bansal; F. George Njoroge; Malcolm MacCoss
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- French
- Weight
- 543 KB
- Volume
- 51
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
A general synthetic approach to 4,6-substituted thiazole[4,5-c]pyridines, involving a novel one-pot thiol deprotection-cyclization key step, is described.
π SIMILAR VOLUMES
Novel substituted thiazole[4,5-c]pyridines have been synthesized in good yields from unsubstituted thiazole[4,5-c]pyridine using direct C-H coupling reactions and N-oxide rearrangement chemistry.
## Abstract magnified image The preparation of oxazolo[4,5β__c__]pyridine and 6βazaindole from 4βbromoβ3βpivaloylaminopyridine (**8**) is reported. The oxazolopyridine 2β__tert__βbutylβoxazolo[4,5β__c__]pyridine (**9**) was successfully prepared from **8** in 78% yield by a new base/TBAB promoted
## Abstract magnified image A oneβstep synthesis of thiazolo[5,4β__b__]pyridines from an appropriately substituted chloronitropyridine and thioamide, or thiourea, is presented. In particular, the reaction was used to prepare a large number of 6βnitrothiazolo[5,4β__b__]pyridine derivatives, bearing
Lithiation with LDA of thiazolo[5,4-blpyridines occurs regioselectively on the position in the pyridine ring.