Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721844Generated: October 25, 2026

Methyl 9-bromononanoate → 6-(N-Allyl-N-cyclohexylamino)-9-(8-methoxycarbonyloctyl)-purine

https://huagongshe.com/reaction/1721844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 9-bromononanoateHCID 554142—
ReactantSodiumHCID 5360545—
ReactantHCID 13851922HCID 13851922—
SolventIsopropanolHCID 3776—
Product6-(N-Allyl-N-cyclohexylamino)-9-(8-methoxycarbonyloctyl)-purineHCID 2002997637%

Reaction Steps

To a solution of 0.7 g. (30 mmole) sodium in 100 ml. propan-2-ol are added 7.7 g. (30 mmole) 6-(N-allyl-N-cyclohexylamino)-purine (compound of Example 8 j), the reaction mixture is heated to 40° C. for 10 minutes, 7.5 g. (30 mmole) methyl 9-bromononanoate are added thereto, the reaction mixture is heated under reflux for 16 hours and evaporated and the residue is taken up in water, extracted with dichloromethane, dried and evaporated. After chromatography on silica gel (elution agent: dichloromethane/methanol 95:5 v/v), there are obtained 4.8 g. of the title compound (37% of theory) in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04853386
Source datasetuspto-grants-1989_08
ORD IDord-96d6df8cdf174eaeb41a244b4d4263ab
Source noteuspto-grants-1989_08