HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Chloropurine riboside → HCID 15611205, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Chloropurine riboside | HCID 93003 | — |
| Reactant | Cyclohexanemethylamine, 1-phenyl- | HCID 205110 | — |
| Product | HCID 15611205 | HCID 15611205 | 42.4% |
Reaction Steps
(1-Phenylcyclohexyl)methylamine (1.80 g, 8 mmol) as prepared below, and 6-chloropurine riboside (2.36 g, 8 mmol) are reacted as described in Example 1. The solvent is removed under reduced pressure, and the residue dissolved up in CHCl3 and washed with water and dried (MgSO4). The solvent is removed under reduced pressure and the residual white foam is purified on silica gel chromatography eluting with 10% MeOH in CH2Cl2 to give N6-((1-phenylcyclohexyl)methyl)adenosine (1.49 g, 42%) as a white glass m.p. 87°-9° C. Found: C, 62.22; H, 6.96; N, 15.70%. C23H29N5O4 calculated requires: C, 62.87; H, 6.61; N, 15.95%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04755594 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-652a1ccacd814f8b86b6ed43fbedd285 |
| Source note | uspto-grants-1988_07 |