HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → PD 117519
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Chloropurine riboside | HCID 93003 | — |
| Reactant | (+-)-1-Aminoindan | HCID 123445 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | PD 117519 | HCID 13424663 | 60% |
Reaction Steps
For 20 hours, 1.83 g 6-chloropurine riboside, 0.95 g (R) (-)-1-aminoindane and 0.862 g triethylamine are refluxed in 50 ml absolute ethanol under nitrogen atmosphere. The solvent is evaporated to dryness and residue is treated with 50 ml cold water. The solid material is filtered, dissolved in excess ethanol, and volatiles are evaporated under reduced pressure to remove water. Residue upon treatment with ethanol affords solid material. It is filtered and dried. One more crop of the same material is obtained from the mother liquor yielding 1.46 g (60% of theory) of N(6) [1-(R)-indanyl]adenosine having a melting point of 185°-187° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04693996 |
| Source dataset | uspto-grants-1987_09 |
| ORD ID | ord-9c1a808f6df141b7b8c03a27e7b7b33d |
| Source note | uspto-grants-1987_09 |