Phosphoric Acid → Ancitabine

反応式

[CH:1]1[C:7]([NH2:8])=[N:6][C:4](=O)[N:3]([C@@H:9]2[O:13][C@H:12]([CH2:14][OH:15])[C@@H:11]([OH:16])[C@@H:10]2[OH:17])[CH:2]=1.[C@@H]1(N2C=CC(N)=NC2=O)O[C@H](CO)[C@@H](O)[C@H]1O.P(=O)(O)(O)O>>[CH:1]1[C:7](=[NH:8])[N:6]=[C:4]2[N:3]([C@@H:9]3[O:13][C@H:12]([CH2:14][OH:15])[C@@H:11]([OH:16])[C@@H:10]3[O:17]2)[CH:2]=1

参加物

反応物 3

HCID 1004Phosphoric Acid

HCID 6175Cytidine2 回

HCID 6253Cytarabine

生成物 1

HCID 25051Ancitabine

実験手順

Roberts et al (J. Org. Chem. 32, 816 (1967)) teach the production of cytarabine from cytidine (or from 2'(3')-cytidylic acid). Specifically, cytidine is reacted with phosphoric acid at 80° C. for a period of 30 hours to produce a 2,2'-O-cyclocytidine analogue intermediate. This intermediate is then hydrolyzed at a pH of 9 utilizing lithium hydroxide to produce the 3',5'-diphosphate of cytarabine. The diphosphate is then treated with magnesium chloride, ammonium chloride and concentrated ammonium hydroxide, and thereafter purified by column chromatography to yield pure cytarabine. The overall yield of pure cytarabine is limited to 53% based on the unrecovered portion of the starting cytidine.