HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 86592810, compound → HCID 12042145, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 86592810 | HCID 86592810 | — |
| Reactant | HCID 86592811 | HCID 86592811 | — |
| Product | HCID 12042145 | HCID 12042145 | — |
Reaction Steps
Amination of compound 5 or 6 to obtain the 8-alkylamino-2-iodoadenosines 7–10 was generally as follows: to 8-bromo-2-iodoadenosine (5) or 2′,3′,5′-tri-O-acetyl-2-iodo-bromoadenosine (6) (0.17 mmol) the appropriate alkylamine was added (excess) and the mixture was stirred overnight at room temperature. The reaction mixture was concentrated in vacuo and the product was crystallised from water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07112574B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-40d74305e5dc49679e259524a8413d0b |
| Source note | uspto-grants-2006_09 |