反应 #1255523
相关文献 (1)
openreactiondata ↗doi:10.6084/m9.figshare.5104873.v1; patent:US09428456B2
反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound is prepared according to the reactions described above starting from 3-nitro-benzaldehyde and piperidine-4-carboxylic acid isobutyl-methyl-amide yielding after reductive amination 1-(3-nitro-benzyl)-piperidine-4-carboxylic acid isobutyl-methyl-amide; LC-MS A: tR=0.61 min; [M+H]+=366.35 followed by reduction with stannous chloride the title compound LC-MS A: tR=0.48 min; [M+H]+=304.24. The title compound is prepared
来源 ID: ord-e60ca1d1f2554e7da83dac20fd0787d2