Safar, M. published the artcileNitrogen compounds of adamantane. VII. New preparation of 7-nitro-1,3,5-triazaadamantane and derivatives by hydrogenation and ozonization, Product Details of C7H14N4, the publication is Collection of Czechoslovak Chemical Communications (1975), 40(7), 2179-82, database is CAplus.
Reflux of hexamethylenetetramine, 80% aqueous EtOH, 98-100% HCO2H, and MeNO2 gave 65% I (R = NO2) which was hydrogenated (over PtO2 or Pd/C in EtOH) to I (R = NH2) or (over Pd/C in H2O) to I (R = NHOH). Quaternization of I (R = NO2) with MeI or EtI gave 7-nitro-1,3-diaza-5-alkylazoniaadamantane iodide (alkyl = Me, Et). Reaction of I (R = NO2) with O3 in H2O or 30% H2O2 in AcOH gave the corresponding N-oxide. I (R = NHCH2CN and NHCH2CH2NH2) were also prepared
Collection of Czechoslovak Chemical Communications published new progress about 14707-75-6. 14707-75-6 belongs to catalysis-chemistry, auxiliary class Triazinanes, name is 1,3,5-Triazaadamantan-7-amine, and the molecular formula is C7H14N4, Product Details of C7H14N4.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia