2-Chloro-5-nitropyridine → HCID 67536866, compound

Participants

Reaction Steps

This compound was prepared with the same method described before by using 2-methoxy-1-methylethylamine and 2-chloro-5-nitro-pyridine to give N-(2-methoxy-1-methylethyl)-2-amino-5-nitro-pyridine. LCMS calcd for C9H13N3O3 m/e 211.22, obsd 210.2 (AP, M−H). The nitro compound was hydrogenated under the same condition described before to give N2-(2-methoxy-1-methylethyl)-2,5-diaminopyridine.

Provenance & Evidence