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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362608Generated: October 25, 2026

Dicyclohexylcarbodiimide → (R)-9-[4-(N-BOC-L-isoleucyloxy)-2-(stearoyloxymethyl)butyl]guanine

https://huagongshe.com/reaction/362608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactanttert-Butoxycarbonyl-L-isoleucineHCID 2724762—
Reactant(R)-9-[4-hydroxy-2-(stearoyloxymethyl)butyl]guanineHCID 135481053—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
Product(R)-9-[4-(N-BOC-L-isoleucyloxy)-2-(stearoyloxymethyl)butyl]guanineHCID 136377418—

Reaction Steps

(R)-9-[4-Hydroxy-2-(stearoyloxymethyl)butyl]guanine (135 mg, 0.26 mmole) and N-BOC-L-isoleucine (180 mg, 0.78 mmole) was coevaporated with dry DMF twice and dissolved in the same solvent (3.5 ml). To the solution was added 1,3-dicyclohexylcarbodiimide (160 mg, 0.78 mmole) and 4-dimethylaminopyridine (4.8 mg, 0.039 mmole). After reaction for 18 hours, the reaction mixture was filtered through Celite and worked up in a conventional manner. The product was isolated by silica gel column chromatography, eluting at 5% MeOH in CH2Cl2. (Yield 160 mg)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869493
Source datasetuspto-grants-1999_02
ORD IDord-a5f5c2d624084335af5f319bdf58ce80
Source noteuspto-grants-1999_02