HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopentylamine → HCID 15051904, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopentylamine | HCID 2906 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 15682117 | HCID 15682117 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15051904 | HCID 15051904 | — |
Reaction Steps
To 1.5 g of 6-chloro-9-(2'-O-methyl-β-D-ribofuranosyl)-9H-purine and 510 mg of cyclopentylamine, 1.5 ml of triethylamine and 70 ml of ethanol were added. The solution was refluxed with heating for several ten minutes to 8 hours. After washing the residue with water, methanol was added and the solution was concentrated to dryness again. The residue was recrystallized with ethyl acetate to give N6 -cyclopentyl-2'-O-methyladenosine (Compound 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04985409 |
| Source dataset | uspto-grants-1991_01 |
| ORD ID | ord-0fad2de14e9b4da19001d0fbcc33a0d7 |
| Source note | uspto-grants-1991_01 |