HRID1905368

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID222

Ammonia gas

H3N

结构：CC(=O)OC[C@H]1O[C@@H](n2cnc3c(Cl)nc(N)nc32)[C@@](O)(C(C)=O)[C@@]1(O)C(C)=O

HCID86743189

未命名化合物

PRODUCTS

生成物

结构：Nc1nc(N)c2ncn([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c2n1

HCID72200

2-Aminoadenosine

C10H14N6O4

PROCEDURE

实验过程

The 6-position of 2-amino-6-chloro-9-(2,3,5-O-triacetyl-β-D-ribofuranosyl)-9H-purine was aminated by ammonia to give 2-aminoadenosine. In the same manner as Example 1 [METHOD 1], 2-aminoadenosine was methylated to give 2-amino-2'-O-methyladenosine (Compound 30) and 2-amino-3'-O-methyladenosine (Compound 31).