Eritadenine

Eritadenine

Names
Preferred IUPAC name (2R,3R)-4-(6-Amino-9H-purin-9-yl)-2,3-dihydroxybutanoic acid
Other names Lentysine; Lentinacin
Identifiers
CAS Number	23918-98-1
3D model ( JSmol )	Interactive image
ChemSpider	140628
PubChem CID	159961
UNII	41T27K4B9F
CompTox Dashboard (EPA)	DTXSID00178632
InChI InChI=1S/C9H11N5O4/c10-7-5-8(12-2-11-7)14(3-13-5)1-4(15)6(16)9(17)18/h2-4,6,15-16H,1H2,(H,17,18)(H2,10,11,12)/t4-,6-/m1/s1 Key: LIEMBEWXEZJEEZ-INEUFUBQSA-N InChI=1/C9H11N5O4/c10-7-5-8(12-2-11-7)14(3-13-5)1-4(15)6(16)9(17)18/h2-4,6,15-16H,1H2,(H,17,18)(H2,10,11,12)/t4-,6-/m1/s1 Key: LIEMBEWXEZJEEZ-INEUFUBQBZ
SMILES c1nc(c2c(n1)n(cn2)C[C@H]([C@H](C(=O)O)O)O)N
Properties
Chemical formula	C9H11N5O4
Molar mass	253.218 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Eritadenine is a chemical compound found in

Ring opening of the protected lactone (1), derived from erythrose with sodium phthalimide gives the acid 2; hydrazinolysis (cf Gabriel synthesis) then leads to the amino acid 3. Displacement of chlorine in pyrimidine 4 by the amine function on 3 serves to attach the future imidazole nitrogen and the sugar-derived sidechain (5). The nitro group is then reduced by catalytic hydrogenation, the resulting primary amine is the most basic and is selectively formylated with formic acid. These strongly acidic conditions serve to remove the acetonide protecting group as well (6). Treatment with NaOH then serves to close the imidazole ring, forming eritadenine (7)

References