HCID 19791871, compound → HCID 19791797, compound

Participants

Reaction Steps

2-Butyl-5-hydroxymethyl-4-{N-[(2'-[N-triphenylmethyl-tetrazol-5-yl]biphenyl-4-yl)methyl]amino}pyrimidine, the product of Example 2A, is dissolved in methylene chloride. Excess activated manganese dioxide is added and the reaction mixture is stirred at ambient temperature until the reaction is complete according to TLC analysis. The reaction mixture is then filtered and the filtrate is concentrated in vacuo to give the intermediate 2-butyl-4-{N-[(2'-[N-triphenylmethyl-tetrazol-5-yl]biphenyl-4-yl)methyl]amino}pyrimidine-5-carboxaldehyde. The triphenylmethyl group is removed, as described in Example 1D, to give the title compound.

Provenance & Evidence