Reaction #1255551
Related Literature (1)
openreactiondata ↗doi:10.6084/m9.figshare.5104873.v1; patent:US09428456B2
Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: The title compound is prepared according to the reaction sequence 2.001a-2.001d described above using 5-methylnicotinoyl chloride instead of 4-chlorobenzoyl chloride as in 2.001a and rac-methyl azepane-4-carboxylate instead of ethyl isonipecotate as in 2.001c: LC-MS A: tR=0.48 min; [M+H]+=368.14.
Source ID: ord-1c52142e8a1e42a985678e53309c124c