Sproviero, Jorge F. published the artcileAmmonolysis of acylated 2-amino-2-deoxy-D-glucoses, Name: (3R,4R,5S,6R)-6-(Acetoxymethyl)-3-benzamidotetrahydro-2H-pyran-2,4,5-triyl triacetate, the publication is Anales de la Asociacion Quimica Argentina (1965), 53(3-4), 261-7, database is CAplus.
MeOH-NH3 or MeONa treatment of tetra-O-acetyl-N-acetyl-D-glucosamine nitrile gave no pentose derivatives N-Acetyl-and N-benzoyl-D-glucosamines were stable to MeOH-NH3, but acetylated and benzoylated derivatives gave low recoveries and appreciable quantities of chromogens [including 2-(1,2-dihydroxyethyl)-4-acetamidofuran] and reducing substances, identified on paper chromatog.
Anales de la Asociacion Quimica Argentina published new progress about 14086-92-1. 14086-92-1 belongs to amides-buliding-blocks, auxiliary class Sugar Units,Glu, name is (3R,4R,5S,6R)-6-(Acetoxymethyl)-3-benzamidotetrahydro-2H-pyran-2,4,5-triyl triacetate, and the molecular formula is C4H10O2, Name: (3R,4R,5S,6R)-6-(Acetoxymethyl)-3-benzamidotetrahydro-2H-pyran-2,4,5-triyl triacetate.
Referemce:
https://en.wikipedia.org/wiki/Amide,
Amide – an overview | ScienceDirect Topics