Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216257Generated: November 1, 2026

HCID 86592810, compound → HCID 12042145, compound

https://huagongshe.com/reaction/2216257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86592810HCID 86592810—
ReactantHCID 86592811HCID 86592811—
ProductHCID 12042145HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112574B2
Source datasetuspto-grants-2006_09
ORD IDord-40d74305e5dc49679e259524a8413d0b
Source noteuspto-grants-2006_09