piperidin-4-yl morpholine-4-carboxylate

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The title compound is prepared from (3R,3aR,6R,6aR)-6-(5-(4-bromophenyl)-6-chloro-3-((2-(trimethylsilyl)ethoxy)methyl)-3H-imidazo[4,5-b]pyridin-2-yloxy)hexahydrofuro[3,2-b]furan-3-ol and piperidin-4-yl morpholine-4-carboxylate following a procedure analogous to that described for Intermediate 23. LC (method 1): tR=1.03 min; Mass spectrum (ESI+): m/z=716 [M+H]+.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The title compound is prepared from (3R,3aR,6R,6aR)-6-(5-(4-bromophenyl)-6-chloro-3-((2-(trimethylsilyl)ethoxy)methyl)-3H-imidazo[4,5-b]pyridin-2-yloxy)hexahydrofuro[3,2-b]furan-3-ol and piperidin-4-yl morpholine-4-carboxylate following a procedure analogous to that described for Intermediate 23. LC (method 1): tR=1.03 min; Mass spectrum (ESI+): m/z=716 [M+H]+.

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: The title compound is prepared from (3R,3aR,6R,6aR)-6-(5-(4-bromophenyl)-6-chloro-3-((2-(trimethylsilyl)ethoxy)methyl)-3H-imidazo[4,5-b]pyridin-2-yloxy)hexahydrofuro[3,2-b]furan-3-ol and piperidin-4-yl morpholine-4-carboxylate following a procedure analogous to that described for Intermediate 23. LC (method 1): tR=1.03 min; Mass spectrum (ESI+): m/z=716 [M+H]+.