1422457-72-4

Upstream product

• 22428-87-1 4,4-ethylenedioxycyclohexan-1-ol 
• 1422457-71-3 2-[2-(1,4-dioxaspiro[4.5]dec-8-yloxy)-6-(trifluoromethyl)pyridin-4-yl]propan-2-ol 
• 1379375-72-0 2-[2-chloro-6-(trifluoromethyl)pyridin-4-yl]propan-2-ol 
• 1196154-43-4 ethyl 2-chloro-6-(trifluoromethyl)isonicotinate 
• 796090-23-8 2-chloro-6-(trifluoromethyl)pyridine-4-carboxylic acid 

Downstream Products

• 1422457-73-5 {1-(cis-4-{[4-(1-hydroxy-1-methylethyl)-6-(trifluoromethyl)pyridin-2-yl]oxy}cyclohexyl)-3-[4-(7-{[2-(trimethylsilyl)ethoxy]methyl}-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]azetidin-3-yl}acetonitrile 
• 1422457-74-6 {1-(trans-4-{[4-(1-hydroxy-1-methylethyl)-6-(trifluoromethyl)pyridin-2-yl]oxy}cyclo hexyl)-3-[4-(7-{[2-(trimethylsilyl)ethoxy]methyl}-7H-pyrrolo[2,3-d]pyrimidin-4-yl)-1H-pyrazol-1-yl]azetidin-3-yl}acetonitrile 

Relevant academic research and scientific papers

JAK1 INHIBITORS FOR THE TREATMENT OF MYELODYSPLASTIC SYNDROMES

This invention relates to JAK1 selective inhibitors, particularly pyrrolo[2,3-d]pyrimidine and pyrrolo[2,3-b]pyridine derivatives, and their use in treating myelodysplastic syndromes (MDS).

CYCLOHEXYL AZETIDINE DERIVATIVES AS JAK INHIBITORS

The present invention provides cyclohexyl azetidine derivatives of formula (I), as well as their compositions and methods of use, that modulate the activity of Janus kinase (JAK) and are useful in the treatment of diseases related to the activity of JAK i